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. 2,266 recalls have been distributed to Maine in the last 12 months.
Showing 47141–47160 of 48,770 recalls
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions, Inc., became aware of a potential problem involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only Recalled by...
The Issue: Superpotent (Single Ingredient) Drug: All BiCNU lots within expiration which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automatic Cutting Needles Recalled by Remington Medical Inc. Due to...
The Issue: Sterility of the product may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Preservative-Free MORPHINE Sulfate Injection Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: I-C Drops Recalled by James G. Cole, Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: The product is being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors...
The Issue: Inspan Compressors may break at weld causing a loss of compression
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREVI Isola System Recalled by Biomerieux Inc Due to The instrument may not...
The Issue: The instrument may not dispense the specimen onto the pre-poured media...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TORQ Sternal Closure Device. The common name is TWISTER Recalled by Kardium...
The Issue: The TORQ Sternal Closure Device, Lot 062711, is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated Recalled by...
The Issue: Embedded iron oxide glass defect which may have the potential to break off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT 16 System Product Usage: The Brilliance 16 Recalled by...
The Issue: Philips was notified that the system logout in software version 2.3.6 is now...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Spectrolyse PAI-1 Recalled by Sekisui Diagnostics Llc Due to...
The Issue: SPECTROLYSE PAI-1 activity assay producing lower than expected absorbance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reumofan Plus Tablets Recalled by Samantha Lynn, Inc Due to Undeclared Drug
The Issue: Marketed without an approved NDA/ANDA: Samantha Lynn Inc. is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves...
The Issue: Trilogy Longevity Constrained Liner devices were packaged in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daniella Mangoes May be identified by Daniella sticker with a Recalled by...
The Issue: Firm is recalling certain lots of Daniella brand mangoes because they may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Neera's Tikka Curry Rich and Creamy All Natural Simmering Sauce Recalled by...
The Issue: The product was recalled due to undeclared sub-ingredients of milk and soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whey Protein Isolate Cross-Flow Microfiltration Recalled by MyoSci...
The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...
Recommended Action: Do not consume. Return to store for a refund or discard.