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. 2,874 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,874 in last 12 months

Showing 741760 of 53,621 recalls

Medical DeviceNovember 7, 2025· Intuitive Surgical, Inc.

Recalled Item: Brand Name: Da Vinci Product Name: da Vinci X Recalled by Intuitive...

The Issue: Due to a software implementation error that allowed instruments arms failing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar Salad...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 7, 2025· Costco Wholesale Corporation

Recalled Item: Costco Item# 19927 Kirkland Signature Caesar Salad Recalled by Costco...

The Issue: The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2025· Teva Pharmaceuticals USA, Inc

Recalled Item: Carton label: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA, Inc...

The Issue: Defective Container - A defect in the side-seal which allows leakage of product.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 7, 2025· Rocket Medical Plc

Recalled Item: Brand Name: Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure...

The Issue: IFU and device kit labeling contains misleading statements leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Rocket Medical Plc

Recalled Item: Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure...

The Issue: IFU and device kit labeling contains misleading statements leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Rocket Medical Plc

Recalled Item: Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure...

The Issue: IFU and device kit labeling contains misleading statements leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Rocket Medical Plc

Recalled Item: Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with...

The Issue: IFU and device kit labeling contains misleading statements leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Rocket Medical Plc

Recalled Item: Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure...

The Issue: IFU and device kit labeling contains misleading statements leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Rocket Medical Plc

Recalled Item: Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with...

The Issue: IFU and device kit labeling contains misleading statements leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2025· Beckman Coulter, Inc.

Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...

The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...

The Issue: Due to a number of modules flashed with a date and time associated with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 6, 2025· VENTURA FOODS LLC

Recalled Item: Publix Deli Carolina-Style Mustard BBQ Sauce Recalled by VENTURA FOODS LLC...

The Issue: foreign objects (black plastic planting material) in granulated onion

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 6, 2025· VENTURA FOODS LLC

Recalled Item: Italian Salad Dressing Recalled by VENTURA FOODS LLC Due to Foreign Object...

The Issue: foreign objects (black plastic planting material) in granulated onion

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2025· Fresenius Kabi USA, LLC

Recalled Item: Famotidine Injection Recalled by Fresenius Kabi USA, LLC Due to Microbial...

The Issue: Microbial Contamination of Sterile Products; out of limit results obtained...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm Recalled by C.R....

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· Bard Peripheral Vascular Inc

Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...

The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2025· C.R. Bard Inc

Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm Recalled by C.R. Bard...

The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing