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 31421–31440 of 53,621 recalls
Recalled Item: Flour sold under the following brands: Golden Temple Durum Atta Flour Blend...
The Issue: The firm was notified by their Co-packer that the product may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...
The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #:...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38 Recalled by...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: Carestream found a single unit where four screws in the assembly were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Logic Fit Tibial Tamp Head Recalled by Exactech, Inc. Due to The firm...
The Issue: The firm determined that the labeling (surgical technique) should be updated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...
The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...
The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer Recalled by Exactech,...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer Catalog #:...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...
The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #:...
The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS software. Recalled by Merge Healthcare, Inc. Due to A...
The Issue: A migrated study that has annotations will display the annotations, but when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GU60A system- Digital X-ray Imaging Systems are intended for...
The Issue: When performing the Stitching function on GU60A system, unintended area is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS software. The firm name on the label is Merge Healthcare...
The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...
The Issue: Presence of foreign substance: The recall was initiated due to black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: D'Allesandro Woodland Foods De-stemmed Birdseye Chiles 1 Recalled by...
The Issue: Trace amounts of undeclared peanut found in product
Recommended Action: Do not consume. Return to store for a refund or discard.