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. 2,536 recalls have been distributed to Maine in the last 12 months.
Showing 5821–5840 of 48,770 recalls
Recalled Item: Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free...
The Issue: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leica HistoCore PEGASUS Tissue Processor Recalled by LEICA BIOSYSTEMS...
The Issue: Poorly processed and/or damaged biopsy tissue specimens on the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE HealthCare CRITIKON ONE-CUF blood pressure cuffs Recalled by GE Medical...
The Issue: Use of the blood pressure cuffs could result in inaccurate non-invasive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...
The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...
The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with...
The Issue: Free T3 Calibrators used with T3 Reagent Packs may produce positively biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ Infusion pump Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for cracks on the mount of the front panel of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the...
The Issue: T3 Reagent Packs used with Free T3 Calibrators may produce positively biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sapropterin Dihydrochloride Powder for Oral Solution 100mg Recalled by Dr....
The Issue: Sub-potent Drug; powder discoloration associated with decreased potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Javygtor (sapropterin dihydrochloride) Powder for Oral Solution 100mg...
The Issue: Sub-potent Drug; powder discoloration associated with decreased potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) NEPHROLOGY PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) CONTINUOUS BLOCK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novalung sensor box is a component of the Novalung Console Recalled by...
The Issue: Issue related to Novalung sensor box, which is a component of the Novalung...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator) Recalled by HeartSine...
The Issue: Automated external defibrillators have a manufacturing issue that could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.