Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,366 recalls have been distributed to Maine in the last 12 months.
Showing 24861–24880 of 27,655 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 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 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: 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 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: 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 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 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 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: 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 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 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: 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: FSE Image Upgrade Kit Recalled by Bio-Rad Laboratories Due to The FSE Image...
The Issue: The FSE Image Upgrade kit (part 92019C) is recalled due to issue related 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: 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: 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: Monoject 100 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 100 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.