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. 2,404 recalls have been distributed to Maine in the last 12 months.
Showing 18161–18180 of 27,655 recalls
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...
The Issue: A defective electrical component in the battery charging circuit in two lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...
The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/4 model number 882479 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...
The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...
The Issue: The bed exit alarm may not function properly if the alarm has been armed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.