Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,862 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,862 in last 12 months

Showing 28012820 of 29,496 recalls

Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· Maquet Cardiovascular, LLC

Recalled Item: Acrobat SUV Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...

The Issue: Deviations in the manufacturing process created a compromise in the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Positioner. Model Number C-XP-5000Z Recalled by Maquet...

The Issue: Deviations in the manufacturing process created a compromise in the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· CORNEAT VISION, LTD.

Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Retroactive; Due...

The Issue: Retroactive; Due to complaints, labeling correction for permanent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD...

The Issue: The connectors may not allow catheters to be inserted as intended if the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· Draeger Medical, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...

The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Shoulder Repair Pack-LF Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Some of the suture packages within the convenience kits contain the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· Draeger Medical, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...

The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Pacer Implant Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Some of the suture packages within the convenience kits contain the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Open Heart CDS Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Some of the suture packages within the convenience kits contain the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively...

The Issue: May Generate Negatively Biased Results When Testing Samples with High...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2024· Karl Storz Endoscopy

Recalled Item: 4.5 x 180 mm Aggressive Cutter Recalled by Karl Storz Endoscopy Due to Due...

The Issue: Due to holes detected in the inner barrier system that may compromise the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2024· Hologic, Inc

Recalled Item: BioZorb Marker. Radiographic soft tissue marker. Recalled by Hologic, Inc...

The Issue: Firm received reports of adverse events/complications that include serious...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2024· Philips Medical Systems Technologies Ltd.

Recalled Item: Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to Recalled by...

The Issue: A software issue affecting Philips Vue PACS may cause incorrect ischemic map...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY-LF Recalled by...

The Issue: Medline is recalling medical convenience manufactured using certain lots of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...

The Issue: A limited number of IV bags have been found to leak during filling.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: Imed Products Imed EVA BAG Recalled by The Metrix Company Due to A limited...

The Issue: A limited number of IV bags have been found to leak during filling.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: SECURE 500 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...

The Issue: A limited number of IV bags have been found to leak during filling.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2024· The Metrix Company

Recalled Item: VYGON 250 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix Company...

The Issue: A limited number of IV bags have been found to leak during filling.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing