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. 1,104 recalls have been distributed to New Jersey in the last 12 months.
Showing 16101–16120 of 53,621 recalls
Recalled Item: 15 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V1500HP OUTLOOK PUMP SET 118-single-use for use with the Outlook Recalled by...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTLOOK PUMP IV SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Pump Add-On Set-single use Recalled by B. Braun Medical, Inc. Due to...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Type Blood Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with Recalled by B. Braun...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Vitrectomy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Ear Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Basic Cataract tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Newborn Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Core Biopsy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Stereotactic Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....
The Issue: Through customer feedback, testing a sample with cardiac troponin I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.