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. 2,492 recalls have been distributed to Maine in the last 12 months.
Showing 13661–13680 of 48,770 recalls
Recalled Item: BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack Recalled...
The Issue: Lower than expected results for VITROS¿ Immunodiagnostic Products TSH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electri-Cool II Portable Cold Therapy Unit Recalled by Gentherm Medical, LLC...
The Issue: This recall has been initiated to provide a labeling update with revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar) Recalled by...
The Issue: The U-channel sheaths may cause damage to ProACT implant devices when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ripple Dairy-Free. As It Should Be 8g Plant Based Protein Recalled by RIPPLE...
The Issue: Complaint led investigation found the presence of Bacillus Cereus in one lot...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...
The Issue: Product Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA...
The Issue: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tydemy (drospirenone Recalled by Lupin Pharmaceuticals Inc. Due to Subpotent...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Birds Eye Broccoli Tots Recalled by CONAGRA BRANDS Due to Small rocks and...
The Issue: Small rocks and metal fragments in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SOMATOM Edge Plus-Computed tomography system Model 1026700 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS-Computed tomography system Model 8098027 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge -Computed tomography system Model 10590000 Recalled...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence -Computed tomography systems Model 10590100 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use for all model numbers of the Medtronic Recalled by...
The Issue: There have been reports of stent migration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Direct Amplification Disc Kit Recalled by DiaSorin Molecular LLC...
The Issue: A subset of affected discs are at risk of leakage when it is used more than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper FD series with Software Version Number: 2.1.x- Recalled...
The Issue: Set screws securing the two gliding rods of the Extra Monitors (called 7th...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GERBER Macaroni and Cheese with a side of peas and carrots Recalled by...
The Issue: Beetles were found in the pea ingredient used in the side compartment of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An...
The Issue: (1)Software (SW) versions V1.25.1 and lower may result in TDef (Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Odor-Eaters Spray Powder Recalled by Blistex Inc Due to Chemical...
The Issue: Chemical contamination: Presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enoxaparin Sodium Injection Recalled by Sandoz Inc Due to Temperature Abuse;...
The Issue: Temperature Abuse; temperature excursion during shipping
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.