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. 2,820 recalls have been distributed to New Jersey in the last 12 months.
Showing 7941–7960 of 53,621 recalls
Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....
The Issue: The organization completed a product improvement process to the conjugate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEUS ELISA Parvovirus B19 IgG Test System Recalled by Zeus Scientific, Inc....
The Issue: The organization completed a product improvement process to the conjugate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Positioner Arm may not tighten or lock during normal use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...
The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...
The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril Tablets USP 20 mg Recalled by NCS Healthcare of Kentucky Inc Due...
The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buspirone Hydrochloride Tabs USP 10 mg Recalled by NCS Healthcare of...
The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.