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. 2,658 recalls have been distributed to New Jersey in the last 12 months.
Showing 24881–24900 of 53,621 recalls
Recalled Item: MultiDiagnost Eleva w/ Flat Detector Recalled by Philips North America, LLC...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium / Hydrochlorothiazide Tablets Recalled by Torrent Pharma...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Camber Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; trace amounts of N-Nitroso N-Methyl 4-amino butyric acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Host Defense MycoBotanicals Blood Sugar Recalled by Fungi Perfecti LLC Due...
The Issue: Host Defense MycoBotanicals Blood Sugar, 60 ct. bottles, is recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spine & Trauma 3D Navigation 1.0 (subpart of the system Recalled by Brainlab...
The Issue: In certain occurrences, the affected navigation software application might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape...
The Issue: The device label incorrectly states that the device is sterile. This product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test Recalled...
The Issue: Products were denied Clinical Laboratory Improvement Amendments (CLIA)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL RuSCH One piece Male External Medium Catheter W/O Tape...
The Issue: The device label incorrectly states that the device is sterile. This product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity c Processing Module LN 03R67-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.