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 19261–19280 of 28,641 recalls
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Central Station Recalled by Spacelabs Healthcare Inc Due to The firm...
The Issue: The firm received reports of telemetry SpO2 numerics dropping off the Xhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheridan/CF Recalled by Teleflex Medical Due to Labeling inconsistency -...
The Issue: Labeling inconsistency - units labeled with a 7mm tube may contain a size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...
The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...
The Issue: Sterility of the outer surface of the container compromised due to packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT Computed Tomography X-ray system Recalled by Philips...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance ICT SP Computed Tomography X-ray system Recalled by Philips...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential presence of particulate matter on the blood side of the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...
The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...
The Issue: Encoded with incorrect ranges that are not consistent with the ranges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...
The Issue: An error may occur with the display of dose computed on images other than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Algovita Spinal Cord Stimulation System Recalled by Nuvectra Due to Nuvectra...
The Issue: Nuvectra is conducting a recall due to two clinical risks that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.