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.
Showing 12081–12100 of 53,621 recalls
Recalled Item: Olopatadine HCl Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artificial Tears Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP Deviations:
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olopatadine HCl Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: CGMP Deviations:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OneLIF Torque Limiting Adapter Recalled by Novapproach Spine LLC Due to The...
The Issue: The torque limiting adapter may not stay locked inside of the ratcheting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion¿ Indirect Decompression System (IDS) Model Numbers and Size:...
The Issue: Due to Indirect Decompression System devices exhibiting a potential for weld...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASIN SET Recalled by American Contract Systems, Inc. Due to Basin Set...
The Issue: Basin Set labeling error: components within the kit are for the Single Basin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NDC 0363-6171-09 Walgreens Sinus Pressure Recalled by LNK International,...
The Issue: Boxes mislabeled to read "Decongestant Free", but the product contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use Recalled...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAJUNK Continuous Epidural Tray Recalled by Pajunk Medical Systems, L.P. Due...
The Issue: The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 20 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 30 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Sizer Set- sterilization tray and 6 individual sizers Recalled by...
The Issue: IFU was not provided with the Sizer Set sterilization tray Revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.