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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 30621–30640 of 53,621 recalls
Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMI250 Radiofrequency System. Intended to provide heating for the purpose...
The Issue: In some systems, the unit continues to emit RF energy after the PAUSE button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...
The Issue: The heat-shrink insulation tube may split during autoclave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard 24-Hour Oral Care Kit q2 Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard 24-Hour Oral Care Kit q4 Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA...
The Issue: Instruments may, under certain specific circumstances listed below, fail to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended...
The Issue: Two specific lots was incorrectly manufactured containing a UK power adapter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Foods Market PB & J Parfait Made With Greek Yogurt Recalled by Sunneen...
The Issue: Sunneel Health Foods received a call from their customer indicating some of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit Recalled...
The Issue: Specific lots have been reported to produce falsely lower than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...
The Issue: The firm was marketing the Ondamed System in the US without marketing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corporation Due to Lack...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Argatroban Injection Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.