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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 23181–23200 of 48,770 recalls
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salem Sump Dual Lumen Stomach Tube 10 Fr/Ch (3.3 mm) x 36" (91 cm) Recalled...
The Issue: This voluntary recall is being conducted due to incorrect packaging. In one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Complete Knee Solution Femoral Augment Block Distal only Recalled by...
The Issue: Screw is missing from the package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Akorn, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Feast Mode Flavors Garlic Beer Seasoning Recalled by Feast Mode Blending &...
The Issue: Feast Mode Garlic Beer Seasoning is mislabeled as "Gluten Free"
Recommended Action: Do not consume. Return to store for a refund or discard.