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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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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. BREAST AUGMENTATION b. BREAST REDUCTION CDS c. CUH ABDOMINO
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. ENDOSCOPY-LF b. SEPTO/ENDO
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: GENERAL ENDOSCOPY
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. LAPAROTOMY CDS-LF b. LAPAROSCOPY CDS-LF c. BASIC LAPAROSCOPY CDS
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. MINOR/BREAST BIOPSY-LF b. BREAST BIOPSY-LF
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. EAR CDS-LF b. SINUS CDS-1 c. ZALE FESS CDS d. ZALE OTOLOGY CDS e
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. RHINOPLASTY PACK b. OSC OTOLOGY PACK-LF c. RHYZOTOMY
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. ORAL SURGERY PACK-LF b. EXTRACTION PACK c. ORAL SURGERY PACK
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. BREAST BIOPSY PACK-LF b. BREAST BIOPSY PACK c. LAPAROTOMY PA
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. PORT/TRACH INSERTION CDS-3 b. RESIDENT DERM SURG PACK c. THR
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. EP LAB PACEMAKER PACK b. OPEN HEART CDS c. OPEN HEART CDS d. AAA
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: a. CARDIAC CATH PACK-LF; b. ANGIOGRAPHY-NS-LF; c. EP BA
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls FEMORAL ARTERY PACK-LF. Sterile Procedural Tray
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls UNIVERSAL CORE DR RUNNELS PACK. Sterile Procedural Tray
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Tray, labeled as the following: a. PAIN SERVICE PACK-LF; b. LOCAL BASIC
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls LOCAL PACK. Sterile Procedural Tray.
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls TRACH PACK. Sterile Procedural Tray.
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 15, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls ANCILLARY PACK-LF. Sterile Procedural Tray.
Hazard: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
Hazard: The recall is due to observed intra-operative screw failure. When pre-drilled with ¿1.3mm drill bit for ¿2.0mm screws and ¿1.6mm drill bit for ¿2.4mm we have observed screw failure due to excessive torque.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE UNITE FOOT & ANKLE Screw, Polyaxial Locking, Mini T8 (2.0x8mm), REF MMSL2008
Hazard: The recall is due to observed intra-operative screw failure. When pre-drilled with ¿1.3mm drill bit for ¿2.0mm screws and ¿1.6mm drill bit for ¿2.4mm we have observed screw failure due to excessive torque.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE UNITE FOOT & ANKLE Screw, Non-Locking, Mini T8 (2.0x8mm), REF MMSN2008
Hazard: The recall is due to observed intra-operative screw failure. When pre-drilled with ¿1.3mm drill bit for ¿2.0mm screws and ¿1.6mm drill bit for ¿2.4mm we have observed screw failure due to excessive torque.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as TOTAL KNEE KIT, 1 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as THEDA CLARK TOTAL KNEE CDS, 1 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as LAPAROTOMY CDS, 2 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 8, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Non-sterile procedural trays labeled as CRANI, 2 per case
Hazard: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
February 1, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CENTURION MEDICAL PRODUCTS, SILVER ANTIMICROBIAL VAD DRIVE, REF DT18760
Hazard: The kit contained an expired component.
January 18, 2023Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline CISION Sterile Blades. Labeled as follows with corresponding Item Number. a. STERILE BLADE NO. 10 CARBON STEEL
Hazard: Potential of the blade puncturing the outer foil layer causing a breach in the sterile packaging.