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. 2,355 recalls have been distributed to Maine in the last 12 months.
Showing 26661–26680 of 27,655 recalls
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Discs Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the product because the cartridges may contain discs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: The firm is recalling the product due to some cartridges may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...
The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...
The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...
The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...
The Issue: The firm recalled the device after learning of a possible deviation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...
The Issue: There is a potential for epistaxis during use of the Disposable General...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...
The Issue: The recall was initiated because Karl Storz has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...
The Issue: Shipped with incorrect software
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275...
The Issue: Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to On August...
The Issue: On August 15, 2012, Sorin informed consignees via letter of changes made to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERA PEARL 3-in-1 BREAST THERAPY Recalled by Lansinoh Laboratories Inc Due...
The Issue: The Spanish translation on the Instructions for Use (IFU) insert and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUGGERKNOT IN¿GUIDE PUNCH Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation found that the current design of the product allows the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software for Vitrea Recalled by Vital Images, Inc. Due to Vital Images has...
The Issue: Vital Images has found two potential errors in calcium score values in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.