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. 2,301 recalls have been distributed to Maine in the last 12 months.
Showing 42021–42040 of 48,770 recalls
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed...
The Issue: Northern Valley Baking Company did not declare milk or soy on the allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT Intact PTH Calibrators consists of 6 bottles (4.0 mL Recalled by...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Intact PTH Controls consists of 3 x 1 Bottle Recalled by Abbott...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dianeal PD-2 Peritoneal Dialysis Solution with 1.5% Dextrose Recalled by...
The Issue: Non-Sterility: Complaints of leaks and particulate matter identified as mold...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tivicay (dolutegravir) Tablets 50 mg Recalled by Viiv Healthcare Company Due...
The Issue: Cross Contamination with Other Products: Product contains Promacta...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility:Solution leaking through the port cover of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Synthes Hohmann Retractor Recalled by Synthes, Inc. Due to The Synthes...
The Issue: The Synthes Hohmann Retractor was mis-etched on the product and package as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 Radiation Therapy Planning (RTP) System Recalled by Philips...
The Issue: Philips Medical Systems have recently determined that a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AST For the In vitro quantitative determination of AST Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS URIC ACID For the In vitro quantitative determination of Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS BUN UREA NITROGEN For the In vitro quantitative determination Recalled...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Ventilators The Respironics Trilogy 100 system provides continuous...
The Issue: Internal testing revealed a potentially defective component on the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Photofrin (porfimer sodium) for Injection Recalled by Pinnacle Biologics Inc...
The Issue: Stability Data Does Not Support Expiry: Printed expiration date should be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.