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. 2,787 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,787 in last 12 months

Showing 1216112180 of 29,496 recalls

Medical DeviceApril 15, 2020· C.R. Bard Inc

Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...

The Issue: There is potential for a white paper-type residue attached to the catheter.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2020· Becton Dickinson & Co.

Recalled Item: BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For Recalled by Becton...

The Issue: May exhibit increased levels of artifacts which could be difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Philips North America, LLC

Recalled Item: Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The...

The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Philips North America, LLC

Recalled Item: Cardiovascular Monitoring Device accessory - Product Usage: The chest...

The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing