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. 2,680 recalls have been distributed to Alabama in the last 12 months.
Showing 1561–1580 of 28,641 recalls
Recalled Item: Azurion R1.x and R2.x systems Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: A software issue was identified in the internal communication process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...
The Issue: A mechanical component that supports the O2 gantry to the support structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...
The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco MNA with the HexaVue IP Integration System Recalled by Steris...
The Issue: This is a sub-recall of event RES 96885. The supplier identified that during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to GE HealthCare...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA PET/MR Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex Knee System. Model Numbers: KC-50090 Recalled by CORIN MEDICAL, LTD....
The Issue: Investigation has identified that the age of the nylon packaging material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing BD Insyte Autoguard Shielded IV...
The Issue: Medline Industries, LP. is issuing a recall for specific Medline kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroMyst Applicator Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIONE Model 30-0001 UDI-DI code: 03760305400031 The EPIONE¿ device is...
The Issue: Due to a software bug the robotic arm may incorrectly guide the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch 80 Recalled by LTS Therapy Systems, LLC Due to The nonwoven pads...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IontoPatch STAT Recalled by LTS Therapy Systems, LLC Due to The nonwoven...
The Issue: The nonwoven pads in the device do not absorb the saline solution or any...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemodynamics Software Recalled by CHANGE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo Software Recalled by CHANGE HEALTHCARE...
The Issue: Due to complaints, software update may cause software to unexpectedly shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....
The Issue: Devices contain potentially out-of-specification levels of endotoxins and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.