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. 2,508 recalls have been distributed to Alabama in the last 12 months.
Showing 19881–19900 of 28,641 recalls
Recalled Item: VS II Aliquoter System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 701 Post-Analytical Unit calculator/data processing module Recalled...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 471 centrifuge unit calculator/data processing module Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSD 800 Sorting System calculator/data processing module Recalled by Roche...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A Recalled by...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 512 Pre-Analytical Instrument calculator/data processing module...
The Issue: Roche has received four reports of injury caused by the sharp edge of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...
The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in...
The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...
The Issue: The STAT priority icon was not displayed in the Study List when the study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...
The Issue: Software malfunction; The action being taken due to the device becoming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.