AVID Medical Recalls
172 recalls on record · August 24, 2016 to August 12, 2026 · Medical Devices
Recalls by year
16
17
18
20
21
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.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom NEURO PK convenience kits, Item Code: LGHM021-08
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom MINOR PROCEDURE 6A convenience kits, Item Code: MADN032-01
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom LOWER EXTREMITY convenience kits, Item Code: LGHM038-03 and LGHM038-04
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom LAMINECTOMY PACK convenience kits, Item Code: MADN013-02
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits, Item Code: MADN011-02
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom GYN LAPAROSCOPY convenience kits, Item Code: LGHM013-06 and LGHM013-07
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom GENERAL PACK convenience kits, Item Code: LGHM041-06 and LGHM041-08
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom EXTREMITY PACK convenience kits, Item Code: MADN012-01 and MADN012-02
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom ELECTRO PHYSIOLOGY PK convenience kits, Item Code: LGHM033-04
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom CATH PACK convenience kits, Item Code: LGHM036-14
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom ORTHO TRAY convenience kits, Item Code: LGHM004-07 and LGHM004-08
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom HEART CATH TRAY convenience kits, Item Code: LAKC022-06
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom PACEMAKER TRAY convenience kits, Item Code: LAKC020-08 and LAKC020-09
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom OBSTETRICAL PACK convenience kits, Item Code: HLDH008-04
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom DJ'S VASCULAR/NEURO TRAY convenience kits, Item Code: AV010930-12
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom DAVINCI PACK convenience kits, Item Code: ADVU037-09
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
February 21, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID Medical QA Pack AV10654-10
Hazard: The swab stick collection device provided in a convenience kit expires prior to the kit expiration date.
April 26, 2017Medical DevicesFDA
Avid Medical, Inc. recalls Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory hematology studies including but not limited to
Hazard: Avid Medical Inc has received a complaint was received from an end-user indicating the vacutainer component 519700 (BD: 367863) expiring 12/16 was discovered inside of a kit labelled with an expiration date after 12/16. Upon receipt of complaint, AVID Medical promptly initiated an internal investigation and root cause analysis. Investigation found mixed component lots were contained in product 519700 component case. This occurrence resulted in the incorrect lot number and expiration being attributed to all work orders produced using the affected component. This issue was immediately contained and corrected. A full inventory analysis was conducted reviewing all vacutainer component inventories. The issue was found to affect a total of five vacutainer components.
August 24, 2016Medical DevicesFDA
Avid Medical, Inc. recalls MAMMOGRAPHY
Hazard: Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
August 24, 2016Medical DevicesFDA
Avid Medical, Inc. recalls PEDIATRIC KIDNEY BIOPSY TRAY
Hazard: Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
August 24, 2016Medical DevicesFDA
Avid Medical, Inc. recalls Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
Hazard: Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
August 24, 2016Medical DevicesFDA
Avid Medical, Inc. recalls Convenience Kits, MOHS "OPENING" PROCEDURE TRAY
Hazard: Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.