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 20501–20520 of 53,621 recalls
Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Recalled by...
The Issue: A high frequency output (2 MHz) has not been cleared for distribution in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips...
The Issue: There were unknown bioburden levels prior to sterilization, which may affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprout Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mixed Greens 4 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spring Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Red Clover 4 oz Recalled by Chicago Indoor Garden, Inc. Due to Potential E....
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...
The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PreludeSYNC DISTAL Radial Compression Devices Recalled by Merit Medical...
The Issue: During the sterilization of radial compression devices, some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...
The Issue: Updated Instructions For Use- to contraindications and potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...
The Issue: Intermittent failure of a signal being sent to a monitor from the touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...
The Issue: As part of an investigation into a biocompatibility test discrepancy where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...
The Issue: The specified reagent packs exhibit an increase in the frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...
The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.