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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 22621–22640 of 48,770 recalls
Recalled Item: Discovery IQ Product Usage: The systems are intended for head Recalled by GE...
The Issue: GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula Recalled...
The Issue: Packaged with an incorrect size inner cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...
The Issue: Incorrect needle length and gage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...
The Issue: The optional Vacuum Unit may stop working and display the failure message...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indian Herb Paste (a dietary supplement) Ingredients: Galangal Recalled by...
The Issue: Unapproved new drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Life-Line tm Catalytic Activated Energy Water Recalled by McDaniel Life-Line...
The Issue: Unapproved new drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Watermelon Recalled by World Waters, LLC dba WTRMLN WTR Due to Cold Pressed...
The Issue: Cold Pressed Juice Watermelon WTRMLN WTR Original 12 packs due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...
The Issue: Table tilts without operator involvement as a result of liquid spilling into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...
The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mometasone Furoate Cream Recalled by ACP Nimble Buyer, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Baby Gripe Water herbal supplement with organic ginger and fennel...
The Issue: Presence of an undissolved ingredient, citrus flavonoid.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...
The Issue: Frayed pieces of the mounting card being inside the primary packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Gel Hand Sanitizer (Ethyl Alcohol 70%) Recalled by Ecolab Inc Due to...
The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%) Recalled by Ecolab Inc...
The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advanced Gel Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc Due...
The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc...
The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.