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. 2,787 recalls have been distributed to New Jersey in the last 12 months.
Showing 11421–11440 of 29,496 recalls
Recalled Item: Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description):...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere iScreen Multi Drug Detection (AMT Item Number/ AMT Description):...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oratect III Oral Fluid Drug Screen Device (AMT Item Number/ Recalled by...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Check 1 Panel Drug Cup: (THC) Recalled by Ameditech Inc Due to Various...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...
The Issue: Due to a supplier error where a portion of the raw material was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Mobility Vivacit-E Bearing Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The outer package is labeled as a Size C 38 mm, however, the implant inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 850 Model Number: H3907AD Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Model # H3101RH Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Model # H3100AS Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM670 Pro Model # H3100XB Recalled by GE Healthcare, LLC Due to...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 CZT Model # H3906CW Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM 830 Model # H3910AC Recalled by GE Healthcare, LLC Due to Rotor bearing...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery 670 DR Model # H3100BT Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Recalled by GE Healthcare, LLC Due to Rotor bearing screws were...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.