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 23501–23520 of 29,496 recalls
Recalled Item: Winco Designer Care Cliner w/Swing Arms - with Nylon Casters Oncology...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Care Cliner X-Large - with Steel Casters Oncology Recalled by Winco...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Elite Care Cliner w/Swing Away Arms Standard - with Recalled by Winco...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco XL Convalescent Recliner - with Steel Casters Long term Recalled by...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Drop Arm Care Cliner Standard - with Steel Casters Oncology Recalled...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Drop Arm Care Cliner Standard - with Nylon Casters Oncology Recalled...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Care Cliner Standart - Steel Casters Oncology Recalled by Winco Mfg.,...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW-i Anesthesia System The FLOW-i Anesthesia System is intended for...
The Issue: In some Flow-i Anesthesia Systems, patient cassette can get dislodged which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Winco Designer Care Cliner - with Nylon Casters Oncology Recalled by Winco...
The Issue: Shipment of foam for chairs was received classified as Fire Retardant but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Handling System (Motion Control Software) Recalled by Viewray...
The Issue: ViewRay received a report that the couch moved unexpectedly into the bore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier Recalled...
The Issue: Customer complaints were received of power to the unit ceasing and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Request Distributor (TRD 1.3 and TRD 1.4) Recalled by Dako North...
The Issue: If a user requests slides from the LIS or TPID, then updates a request by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...
The Issue: A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProTrack Microcatheter Recalled by Baylis Medical Corp * Due to Baylis...
The Issue: Baylis Medical Company is recalling two lots of ProTrack Microcatheter due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE:...
The Issue: Potential for clear extension tube to separate from the hub, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Recalled by...
The Issue: Blood foaming was found during evaluation of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number...
The Issue: A limited number of VPS G4 Consoles are being recalled due to noncompliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: Potential for clear extension tube to separate from the hub, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTIPLEX Continuous Peripheral Nerve Block Tray Recalled by B. Braun...
The Issue: There is a potential for a hole to be present in the outer tray of a limited...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle....
The Issue: Product is being recalled due to complaints of cracked frames.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.