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. 2,862 recalls have been distributed to New Jersey in the last 12 months.
Showing 2261–2280 of 53,621 recalls
Recalled Item: SwabFlush Prefilled Syringe with ICU Medical SwabCaps Recalled by MEDLINE...
The Issue: SwabFlush syringes are affected by the ICU Medical recall of their SwabCap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PhaSeal Injector Luer (N30C) Recalled by BD SWITZERLAND SARL Due to...
The Issue: Closed system drug transfer devices were shipped to the U.S. market without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 90 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 55 Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStar 60A Plus Filter. Bidirectionally breathing system filter. Recalled...
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter....
The Issue: Reports of slow increase of CO2-curve when gas sample is taken from the gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity XR Toric Contact Lens Recalled by CooperVision, Inc. Due to Lens...
The Issue: Lens blisters may have an incomplete or leaking seal which may render them...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biofinity Toric Multifocal Contact Lens Recalled by CooperVision, Inc. Due...
The Issue: Lens blisters may have an incomplete or leaking seal which may render them...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...
The Issue: Product may contain foreign objects of metal origin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...
The Issue: Product may contain foreign objects of metal origin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: a. Wegmans brand Mini Muffins Recalled by Wegmans Food Markets, Inc. Due to...
The Issue: Product may contain foreign objects of metal origin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vitamins B12 dietary supplement Raspberry Flavored sold under the following...
The Issue: Undeclared Peanuts. The firm was notified by their supplier, that the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) Recalled by...
The Issue: Reports of IVUS catheter and guide wire entanglement during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA...
The Issue: Estrone RIA kit lots may rarely give falsely high patient results which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL Recalled by Johnson & Johnson Vision...
The Issue: Due to defects (bubbles/voids) identified during standard finished goods testing
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 Recalled by...
The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Recalled by Vita...
The Issue: Contains undeclared peanut
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Famciclovir Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Presence...
The Issue: Presence of Foreign Substance- Black hair strand found attached to a tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pitavastatin Tablets Recalled by Orient Pharma Co., Ltd. Yunlin Plant Due to...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pitavastatin Tablets Recalled by Orient Pharma Co., Ltd. Yunlin Plant Due to...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.