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. 1,087 recalls have been distributed to Maine in the last 12 months.
Showing 6421–6440 of 27,655 recalls
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGACY SMARTBASE Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Non-engaging abutments were distributed without FDA clearance; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Sign Sensor 2 Recalled by SenTec AG Due to The sensors may experience an...
The Issue: The sensors may experience an out-of-box failure because after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy...
The Issue: The inner needle of the Sertera device is either detaching or discharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVent EVO2 Recalled by Philips Respironics, Inc. Due...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Environmental...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: The Trilogy Evo Universal ventilator provides continuous or intermittent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...
The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel multiplexed nucleic acid real-time...
The Issue: Faulty cartridges in the lot could result in false test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelli-C Recalled by NRT X-RAY A/S Due to There is a potential that the...
The Issue: There is a potential that the drive shaft in the detector up/down (IDE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelli-C Recalled by NRT X-RAY A/S Due to There is a potential that the...
The Issue: There is a potential that the drive shaft in the detector up/down (IDE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Recalled by HeartSine Technologies Ltd Due to Single use battery...
The Issue: Single use battery and electrode cartridge may be rendered inoperable due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w Echo PS 4.5" Circle A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...
The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4.5" Circle with Echo PS- A low profile Recalled by Davol,...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.