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MEDLINE INDUSTRIES, LP - Northfield Recalls
822 recalls on record · December 29, 2021 to October 1, 2025 · Drugs, Medical Devices
Recalls by year
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25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE M1S0179 STRL TAPE/PEN PACK, Product Code P519582A
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300), Product Code 67335
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Manual surgical kits labeled as: a) HEGAR UTERINE DILATOR, 11-12MM, STERILE, Product Code HUD112ST; b) ST
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Manual surgical kits labeled as: a) STERILE S/B WIRE SCISSOR, Product Code 65140; b) SHARP/SHARP SCISSORS
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP, Product Code 15MLVLCP; b) STERILE 9X12 R
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion PICC LINE SECUREMENT KIT, Product Code IVS565
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion STERILE #16 RUBBER BAND, Product Code EB16
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) SUTURE REMOVAL TRAY, Product Code TRI55405; b) SUTURE REMOVAL SET, Prod
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S SCISSOR (SS5031), Product Code 65145; b) STERILE S/
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) STERILE ALLIS TISS FCP 10", Product Code I68905; b) VAGINAL REPAIR KIT
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) ST. VIRTUS SPLINTER FORCEP 6" (SF8246), Product Code 66580; b) DEBRIDE
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225; b) ST. KEL
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173), Product Code 66520; b) STERILE TOWEL CLAM
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Curette kits labeled as: a) STERILE BUCK EAR CURETTE "00" (25697), Product Code 66745; b) STERILE "1" EAR
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV MOSQUITO HEM
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Forcep kits labeled as: a) STERILE F/P SPLINTER FORCEP (SF6141), Product Code 66165; b) STERILE WEBSTER NEED
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE, Product Code 66825; b) STERILE PAS #3 BLADE
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion hook kits labeled as: a) STERILE SKIN HOOK FINE (EA3975F), Product Code 66660; b) STERILE SMALL 2 PRONG SKI
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion retractor kits labeled as: a) STERILE 6-1/2" SENN RETRACTOR (ST7185), Product Code 66795; b) STERILE RAGNEL
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion STERILE ROUND EAR SPECULUM SET (3, 4, 5), Product Code I68505
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion STERILE #5 LARYNGEAL MIRROR(505709), Product Code 67830
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion kits: a) DENTAL INSTRUMENT KIT, Product Code DH760; b) STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125S
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion STERILE BLOOD COLLECTION TUBE,10ML, Product Code 6430ST
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion FCP MAGILL CATH 7.5 IN PED (67575), Product Code 67575
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
April 10, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion STERILE TRACH BRUSH, Product Code 6225ST
Hazard: Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
March 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CVS Health Waterproof Wound Tracking Dressing, REF CVS690330, immediate package contains 1 sterile dressing, 4 in. x 4 i
Hazard: Product failed sterility testing.
March 6, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Kits, trays, and packs labeled as follows: CIRCUMCISION TRAY, REF DYNDA2271
Hazard: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
March 6, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Kits, trays, and packs labeled as follows: BREAST BIOPSY KIT, REF MNS4360
Hazard: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
March 6, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Kits, trays, and packs labeled as follows: a) A C DAILY WET KIT, REF DM405A; b) BWH DAILY DRIVELINE MGMT
Hazard: Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.