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. 2,478 recalls have been distributed to Alabama in the last 12 months.
Showing 23021–23040 of 28,641 recalls
Recalled Item: Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw...
The Issue: A component failure could cause a situation where the applied torque was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD" Medication Cassette Reservoir Recalled by Smiths Medical ASD, Inc. Due...
The Issue: Smiths Medical has become aware of an issue with specific lots of 50mL CADD"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOLUTION MP TIBIAL BASE Recalled by Microport Orthopedics INC. Due to Some...
The Issue: Some units of the EVOLUTION Tibial Base was affected by a casting tool issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard 100% Latex-Free Urinary Drainage Bag with Anti- Chamber and Recalled by...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1...
The Issue: If the patient sits on either wing, not squarely on the center section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Power supply malfunction complaints related to suboptimal thermal management.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Proteus XR/a with wall stand model number 2260354. Recalled by...
The Issue: Potential breakage of the steel cable which supports the bucky device in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Precise Treatment Table Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible to position the Treatment Table with errors greater than 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis Recalled...
The Issue: An increase in complaints of loosening and radiolucent lines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The dual port with catheters was not covered under FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...
The Issue: Potential failure of the caster mounting hardware, which may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher Brand Gel Infant Heel Gel Warmers Recalled by CooperSurgical, Inc....
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice WarmGel Infant Heel Warmer Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Passport V Monitor Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: An issue has been identified with Passport V Monitors invasive blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAX-TL 9.0 x 7.0 mm Implant Recalled by Southern Implants, Inc Due to Z-MAX...
The Issue: Z-MAX Implant, 9mm diameter, 7mm length labeled package, catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.