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. 2,520 recalls have been distributed to Maine in the last 12 months.
Showing 10221–10240 of 48,770 recalls
Recalled Item: BD Pyxis MedBank System - Product Label/labeling pending Recalled by...
The Issue: Due to customer complaints related to the MedBank software which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Steam Test Pack (20 Tests and 20 controls) Item Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Steam Test Pack (20 Tests and 5 controls) Item Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: By Heart Whole Nutrition Infant Formula Recalled by ByHeart, INC. Due to...
The Issue: Infant formula potentially contaminated with Cronobacter sakazakii
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Recalled by NCH Life...
The Issue: CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thiamine Hydrochloride 200 mg/2mL (100mg/mL) Recalled by McGuff Compounding...
The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL) Recalled by McGuff...
The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...
The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...
The Issue: There is an increased chance that the tests from affected lots may give...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.