Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,509 recalls have been distributed to Alabama in the last 12 months.
Showing 18781–18800 of 28,641 recalls
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: 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: 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: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings 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: 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: 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: 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: 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 (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: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...
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.
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: 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: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...
The Issue: Incorrect device was packaged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...
The Issue: There has been an increase in the number of complaints regarding bent or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...
The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: The mobile-specific instructions was not shipped to a limited population of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.