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. 2,696 recalls have been distributed to New Jersey in the last 12 months.
Showing 20781–20800 of 53,621 recalls
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: 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.
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: All Dietary Supplement manufactured and distributed by ABH Nature's Products...
The Issue: Firm ordered by consent decree to recall all products because the products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COLUMBUS REV F TIBIA OFFSET CEMENTED Recalled by Aesculap Implant Systems...
The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Detect Cotinine Recalled by Polymer Technology Systems, Inc. Due to The...
The Issue: The firm is removing the product from the market after discussions with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selenia Dimensions Mammography System Recalled by Hologic, Inc. Due to The...
The Issue: The recalling firm has received reports from the field of the C-arm on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast Sodium Chewable Tablets Recalled by Macleods Pharma Usa Inc Due...
The Issue: Failed Dissolution Specifications: testing revealed low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Reagent Kit Recalled by Carolina Liquid Chemistries Corp Due to...
The Issue: Labeled for diagnostic use and sold to clinical labs without a 510(k). Firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...
The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LabPro Data Management System Recalled by Beckman Coulter Inc. Due to A...
The Issue: A security-only update was released via remote diagnostics on January 14,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...
The Issue: The action is being taken due to an increase in complaints relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection...
The Issue: Potential for the sterile barrier to be compromised. Products with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...
The Issue: The action is being taken due to an increase in complaints relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens Acne Cleansing Bar Recalled by Shandex Personal Care Manufacturing...
The Issue: Presence of Foreign Substance; Metal contaminant visible in product (screen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COHERENCE Oncologist Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue arises when an offset calculation is followed by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.