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. 989 recalls have been distributed to Maine in the last 12 months.
Showing 29841–29860 of 48,770 recalls
Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...
The Issue: Potential contamination of product with E. coli O157.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...
The Issue: Potential contamination of product with E. coli O157.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dixie Diners' Club Carb Not Beanit Butter Recalled by The SoyNut Butter...
The Issue: Potential contamination of product with E. coli O157.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...
The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...
The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics notified customers that errors were contained in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...
The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xl por st 24.0x220mm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx38cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx48cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 18x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.