Zimmer Recalls
550 recalls on record · September 5, 1978 to July 1, 2026 · Medical Devices, Vehicles
Recalls by year
78
81
82
12
13
14
15
16
17
18
19
21
22
23
24
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Sirus¿ intramedullary nail for tibia, cannulated ¿
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls NCB¿-PH Plate
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls NCB¿-PT lateral proximal 3 hole tibial plate
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls NCB¿ screw ¿ 4.0 self-tapping
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls NCB¿ cancellous screw
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls DTO" Implant
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Dynesys¿ HA Pedicle + set screw
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthru, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Dynesys¿ Revision + set screw
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Dynesys¿ L.I.S. Stabilizing cord Rx, Sterile
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Dynesys¿ Universal spacer 6-45
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Dynesys¿ Set screw M6
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Original M.E. Mueller" Low Profile Cup Sterile, Rx
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls CLS Stem
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Fracture Humeral Head
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Ball taper for humeral stem
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Inverse/Reverse Glenoid Sterile, Rx
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Inverse Humeral Cup
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Zimmer Inverse/Reverse Screw system,
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Revision Humeral stem,7,9,12,14 and Anatomical Shoulder Fracture Humeral stem
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls zimmer Anatomical Shoulder Glenoid S, cemented, sterile; REF 01.04214.340 PE Keeled Glenoid S, cemented, sterile; REF
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Humeral Head
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Fracture Humeral stem
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Anatomical Shoulder" Humeral stem
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls CoCr Head, sterile, Rx
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Wagner cone Prosthesis, uncemented, sterile, Rx
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls Fitmore" Hip Stem
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls MS-30¿ Proximal positioner
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
November 14, 2012Medical DevicesFDA
Zimmer, Inc. recalls MS-30¿ Distal centralizer, cemented, sterile, Rx
Hazard: Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info