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. 2,279 recalls have been distributed to Maine in the last 12 months.
Showing 43921–43940 of 48,770 recalls
Recalled Item: OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture Recalled by Smith & Nephew, Inc....
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture Recalled...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quick Thin (citrus aurantium extract Recalled by Bethel Nutritional...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bethel Advance (bitter orange Recalled by Bethel Nutritional Consulting, Inc...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...
The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...
The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valacyclovir HCl Tablets Recalled by American Health Packaging Due to Subpotent
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ranitidine Hydrochloride Tablets Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Microbial Contamination of Non-Sterile Products: A lot of raw material used...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BEST Slim Recalled by CTV Best Group Due to Undeclared Drug
The Issue: Marketed without an Approved NDA/ANDA: Product contains an undeclared drug,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benztropine Mesylate Injection Recalled by Nexus Pharmaceuticals Inc Due to...
The Issue: Presence of particulate matter: characterized as thin colorless flakes that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mavik¿ trandolapril tablets 4mg Recalled by AbbVie Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Package Insert; product packaged with outdated version...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breaded Recalled by Gourmet Express Marketing, Inc. Due to Packages of...
The Issue: Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.