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. 2,467 recalls have been distributed to Alabama in the last 12 months.
Showing 25841–25860 of 28,641 recalls
Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...
The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...
The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...
The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juno DRF System. Mobile X-ray system These are general Recalled by Villa...
The Issue: It has been discovered that the Air Kerma rate information is inconsistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...
The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...
The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...
The Issue: Under certain circumstances, the Left eye image may be saved as the Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...
The Issue: Arrow is recalling the product due to a labeling inconsistency. One portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is initiating a recall removal of the 4.0mm x 15mm size of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Flo Trac Sensor Model MHD85***" Sterile Recalled by Edwards...
The Issue: The Edwards Lifesciences FloTrac Sensor is being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...
The Issue: The affected lots of the product may contain a contaminant of fungus that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.