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. 2,518 recalls have been distributed to Maine in the last 12 months.
Showing 11281–11300 of 48,770 recalls
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...
The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...
The Issue: Failed Dissolution Specifications: below specification limits for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...
The Issue: Failed Dissolution Specifications: below specification limits for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUSTANGO (Pendenadril Tytrate Blend) Capsules Recalled by Ultra Supplement...
The Issue: Marketed Without an Approved NDA/ANDA: Analytical testing showed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...
The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...
The Issue: Due to a non-sterile component (tape) being place within the sterile portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...
The Issue: Device does not meet regulatory requirements of stability while stationary,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by AVKARE Inc. Due to Labeling: Label Error on...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is Recalled by Alcor...
The Issue: Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Bronchovideoscope Recalled by Aizu Olympus Co., Ltd. Due to...
The Issue: The recalled unit was utilized in a veterinary endoscopy procedure in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Critical Care AB/Getinge Servo-u Ventilator System Recalled by...
The Issue: Ventilators may generate a combination of alarms which may result in loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prednisone Tablets USP Recalled by Strides Pharma Inc. Due to Presence of...
The Issue: Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.