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. 1,855 recalls have been distributed to New Jersey in the last 12 months.
Showing 38221–38240 of 53,621 recalls
Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Phase 3 Tibial Template Left Medial Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Femoral Slap Hammer Product Usage: Instruments...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...
The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters Recalled...
The Issue: Report by a customer of an open package seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beirut Lift Turnip Pickles Imported & Distributed By: Baroody Import...
The Issue: Beirut Lift Turnip Pickles contain undeclared beet root red color.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ottobock Modular Polycentric EBS Knee Joint 3R60 Recalled by Otto Bock...
The Issue: Otto Bock HealthCare GmbH is recalling Modular Polycentric EBS Knee Joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...
The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Sandoz Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; 9 month stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...
The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...
The Issue: Incorrect cannula of the sheath introducer (smaller than intended).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...
The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.