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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 28201–28220 of 53,621 recalls
Recalled Item: Dimension Gentamicin Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...
The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...
The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...
The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets USP Recalled by Sun Pharmaceutical...
The Issue: Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD) Recalled by Canon Medical...
The Issue: It was found when an operator performs a radiography using the wireless flat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...
The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder-Thai Maeng Da Recalled by Viable Solutions,...
The Issue: Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Wheat Chocolate Animal Cookies Recalled by NatureBox, Inc. Due to...
The Issue: While packing from a bulk bin of whole wheat chocolate animal cookies, 2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa...
The Issue: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...
The Issue: There is a potential for the cord to spark and cause a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...
The Issue: Failed Dissolution Specification: Low dissolution outside of specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...
The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...
The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS programmer (Model # 3650) Recalled by St Jude Medical Inc. Due to...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.