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. 2,549 recalls have been distributed to New Jersey in the last 12 months.
Showing 48381–48400 of 53,621 recalls
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Actavis...
The Issue: Failed Dissolution Specifications: This recall is an extension of the recall...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Breakpoint Combo 7 Product Usage:...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan plus Negative Breakpoint Combo 4 Sold outside of US Recalled by...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan plus Negative Urine Combo 4 Sold outside of US Recalled by Siemens...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Combo 2 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan Synergies Plus Negative Urine Combo 1 Product Usage: MicroScan¿...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: Recalled...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan plus Negative Combo 3 Sold outside of US only. Recalled by Siemens...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microscan rapID/S panels NC3.33 Sold in Japan only. Product Usage: Recalled...
The Issue: Confirmed increase in false susceptible and false intermediate misreads for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX Evolution System (Standard Q) The DRX-Evolution System...
The Issue: Carestream received a report of an exposure being initiated without a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vision One Laser System Model GA-0025020 Recalled by Lumenis, Inc. Due to...
The Issue: Lumenis has initiated a recall on certain models of Vision One System due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHECK FastClix Lancing Device. It is intended for use in Recalled by...
The Issue: Internal Roche inspections have revealed that after the lancet is used for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Phenytoin Sodium Capsules Recalled by Amneal Pharmaceuticals of New...
The Issue: Failed dissolution specifications; 18 month CRT
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of assurance of...
The Issue: Lack of assurance of sterility: ineffective crimp on fliptop vials that may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription...
The Issue: Product was labeled as a medical food as opposed to a dietary supplement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XYMOGEN LipiChol (Omega-3 Phospholipid 540 mg) Medical Food Distributed by...
The Issue: Product was labeled as a medical food as opposed to a dietary supplement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Hazelnut Butter 16oz Jar (Unit Recalled by Justin'S Nut Butter Due...
The Issue: Justin's has initiated a voluntary recall of certain lots of its Maple...
Recommended Action: Do not consume. Return to store for a refund or discard.