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. 1,947 recalls have been distributed to New Jersey in the last 12 months.
Showing 20761–20780 of 53,621 recalls
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans...
The Issue: FridaBaby has been made aware through customer reports that the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truliant Splined Stem Extension Recalled by Exactech, Inc. Due to These...
The Issue: These Truliant Splined Stem Extension, 18mm x 120mm were found to have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...
The Issue: CGMP deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...
The Issue: CGMP deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...
The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olmesartan Medoxomil Tablets 20 mg Recalled by Ascend Laboratories LLC Due...
The Issue: cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pioglitazone and Metformin Hydrochloride Tablets Recalled by Macleods Pharma...
The Issue: Subpotent Drug: Out of specification assay result, below specification, for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...
The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000...
The Issue: Potential exists for one or more axes of the robotic stand to become blocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LN 3R70-01 Recalled by Abbott Gmbh & Co. KG Due to Abbott has identified...
The Issue: Abbott has identified potential performance issues for the Alinity ci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply...
The Issue: The recall has been initiated due to potential for overheating or a fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical, Cardiac Rhythm Management Division Due...
The Issue: Past updates to programmers and transmitters may lead some implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...
The Issue: There is an increased risk of false positive Proteus results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....
The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.