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 1281–1300 of 50,591 recalls
Recalled Item: LOGIQ P10 series with software version R4.5.7 Model Number 5877534 Recalled...
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray 2 Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL INC...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESPOCAN Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Set Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azelaic Acid Gel Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP...
The Issue: CGMP Deviations: Market complaints received for gritty texture (grainy)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...
The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...
The Issue: When appending a care plan that contains one or more wave medication orders,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent Recalled by Beckman...
The Issue: Beckman Coulter has identified that there is an increased probability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oral Probe (Product code 02893-000) Recalled by Baxter Healthcare...
The Issue: Affected oral/axillary probes were inadvertently programmed with the rectal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400...
The Issue: Instructions for use for a foot plating system is being updated to remove...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.