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 47721–47740 of 48,770 recalls
Recalled Item: Product is a liquid dietary supplement packaged in white plastic Recalled by...
The Issue: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...
The Issue: The deflector may not move freely on the ventricular catheter. The deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...
The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOGEN-82 (Rubidium Rb 82 Generator) Recalled by Bracco Diagnostics Inc...
The Issue: GMP deviation; Sr-82 levels exceeded alert limit specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clams Recalled by Rhee Brothers Incorporated Due to Frozen clams, product of...
The Issue: Frozen clams, product of S. Korea, may be contaminated with Norovirus.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...
The Issue: The recall was initiated because Advanced Sterilization Products has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...
The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...
The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that the outer carton label of this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...
The Issue: The clear tape, that is intended to aid in the prevention of patients...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leukine sargramostim 5 x 500 mcg/mL vial Recalled by Bayer HealthCare...
The Issue: Impurities/Degradation Products: A confirmed out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.