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. 2,317 recalls have been distributed to Maine in the last 12 months.
Showing 38881–38900 of 48,770 recalls
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HemosIL PT-Fibrinogen HS PLUS Recalled by Instrumentation Laboratory Co. Due...
The Issue: Some vials of HemosIL PT-Fibrinogen HS PLUS, Part No. 0008469810 (various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...
The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...
The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes with Swabs Sterile Pack Recalled by Becton Dickinson &...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes Recalled by Becton Dickinson & Co. Due to The products...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bone Screw Recalled by Zimmer Manufacturing B.V. Due to Analysis of returned...
The Issue: Analysis of returned complaint devices, product in inventory, and device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryogenic probe for cardiac ablation surgery Recalled by Atricure Inc Due to...
The Issue: Affected product may have compromised sterility due to packaging defects. It...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / Recalled...
The Issue: Accuray has become aware of a potential safety issue related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device 20G x1 Recalled by Smiths Medical...
The Issue: Needle is not captured in the needle safety sheath in specific lots.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...
The Issue: During an investigation of instrument logs it was determined that In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Recalled by Roche...
The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.