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 26881–26900 of 29,496 recalls
Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...
The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...
The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...
The Issue: The product was registered and distributed as a Class I medical device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...
The Issue: High inlet water pressure beyond specification and the solenoid valve does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...
The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens issued a customer safety advisory notice and field safety corrective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...
The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...
The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....
The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...
The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SC2316 Recalled by Stelkast Co Due to The firm became aware of an incident...
The Issue: The firm became aware of an incident relating to a breach of sterility in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...
The Issue: A supplied component exhibiting corrosion was built into the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole)...
The Issue: A supplied component exhibiting corrosion was built into the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-852-000 (Console 230V) Product...
The Issue: A supplied component exhibiting corrosion was built into the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: Recalled...
The Issue: A complaint was received of the tips of the Matrix 5.5.mm Left and Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.25 mL LeGoo with 3 Cannula Pouch...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo w/ no Cannula Product...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel- 1.0 mL LeGoo with 3 Cannula Recalled by...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder .5mL Product Number: 10-0050 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo with 3 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.