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. 2,816 recalls have been distributed to New Jersey in the last 12 months.
Showing 9841–9860 of 53,621 recalls
Recalled Item: Pin-Away PYRENTAL PAMOATE (Pyrantel base 50 mg / mL) Pinworm Treatment...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe tussin PM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colic Calm Recalled by Denison Pharmaceuticals, LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safe tussin DM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle Recalled by Kenover...
The Issue: The product is being recalled due to Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MEDLINE THERAHONEY GEL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline issued a recall on TheraHoney Wound Gel due to the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to Device...
The Issue: Device may experience malfunctions due to misalignment of the check valve in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of...
The Issue: Potential for the incorrect size stent-graft than the printed carton label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGACY SMARTBASE Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Non-engaging abutments were distributed without FDA clearance; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy...
The Issue: The inner needle of the Sertera device is either detaching or discharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Sign Sensor 2 Recalled by SenTec AG Due to The sensors may experience an...
The Issue: The sensors may experience an out-of-box failure because after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Tablets Recalled by Glenmark Therapeutics, Inc. Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: some cartons labeled and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phadia 2500EE instrument -Intended for the in vitro semi-quantitative...
The Issue: Higher reported results when running EliA GliadinDP IgG Well on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Recalled...
The Issue: Higher reported results when running EliA GliadinDP IgG Well on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...
The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.