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. 1,120 recalls have been distributed to New Jersey in the last 12 months.
Showing 11561–11580 of 29,496 recalls
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 40cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Recalled by C.A....
The Issue: Sample leaking from the sleeve covering the needle inside the cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 7.5Fr 30cc IAB Recalled...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 35cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 25cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 8Fr 50cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 8Fr 50cc IAB Kit P/N:...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 40cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Recalled by...
The Issue: Kits were packaged with the incorrect size valve peelable introducer. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JINYINSHAN Recalled by Office Depot Inc Due to Test results revealed that...
The Issue: Test results revealed that the KN95 masks failed to filter greater than 95%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The...
The Issue: The catalog ( REF ) number on the peelable inner labels (patient sticker)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Sensis Vibe Hemo system in combination with the MicroPodTM Recalled...
The Issue: The connector linking the EtCO2 module to the HemoBox may break and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE SPECIALIZED ORTHOPEDICS Recalled by Nuvasive Specialized...
The Issue: During explantation, standard removal tools can generate sufficient forces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.