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 26601–26620 of 29,496 recalls
Recalled Item: BIOMET Spine Recalled by Ebi, Llc Due to Polaris Translation Screw Failures...
The Issue: Polaris Translation Screw Failures were recently reported to Biomet Spine....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgicutt fully automated incision making device for bleeding time...
The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...
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 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 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 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: 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: 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: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...
The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.