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 20001–20020 of 28,641 recalls
Recalled Item: Dual Chamber Container fill with gravity/attached transfer sets Recalled by...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...
The Issue: It was reported that the secondary locking mechanism, and its corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...
The Issue: Incorrect values for the volume calculation. Software update VB30B via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Chamber Container fill and transfer sets Recalled by The Metrix Company...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Container fill and transfer sets Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...
The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...
The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...
The Issue: Incorrect CO2 readings with some patient monitors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOCOMP6 High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOCOMP6 XPS High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOCOMP6 XP High Speed Compounder Recalled by The Metrix Company Due to An...
The Issue: An issue was identified after a redesign of the auto compounding device. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product...
The Issue: Certain low-voltage DC power supplies (DCPS) used in these products may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: Analytical...
The Issue: Trigger lock option does not always prevent x-ray generation. Specifically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...
The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is...
The Issue: Devices were incorrectly programmed during manufacturing therefore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoClip AC 8cm 35 Clips (1 Each} Large REF # Recalled by LeMaitre...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # Recalled by LeMaitre...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.