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. 1,062 recalls have been distributed to New Jersey in the last 12 months.
Showing 21541–21560 of 53,621 recalls
Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...
The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm Recalled by Paltop...
The Issue: Some of the implants were packaged with a Standard Platform Cover Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA SYSTEM CONROL N + P (ref. 00678) Recalled by Diagnostica Stago, Inc. Due...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...
The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA UNICALIBRATOR (ref. 00675) Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...
The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...
The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...
The Issue: Labeling mix-up - Indications on product label are incorrect.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breakstones 4% Milkfat Small Curd Cottage Cheese Recalled by THE KRAFT HEINZ...
The Issue: Potential presence of pieces of red plastic and metal that may have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breakstones 4% Milkfat Large Curd Cottage Cheese Recalled by THE KRAFT HEINZ...
The Issue: Potential presence of pieces of red plastic and metal that may have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breakstones 2% Milkfat Lowfat Large Curd Cottage Cheese Recalled by THE...
The Issue: Potential presence of pieces of red plastic and metal that may have been...
Recommended Action: Do not consume. Return to store for a refund or discard.