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. 2,664 recalls have been distributed to Alabama in the last 12 months.
Showing 3461–3480 of 28,641 recalls
Recalled Item: Stryker iBur 4.0mm Diamond Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 4.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube Recalled by Cardinal...
The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 5.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker TMJ Unilateral Implant Recalled by TMJ Solutions Inc Due to...
The Issue: Patient-fitted temporomandibular (TMJ) prothesis contained incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Diamond Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Syringe 60CC Recalled by Cypress Medical Products LLC Due to...
The Issue: Affected syringes lack FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti- Valve...
The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker iBur 3.0mm Precision Round Recalled by Stryker Corporation Due to...
The Issue: Potential for the product to exhibit temperatures higher than specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft Infusion Set Recalled by Unomedical A/S Due to Specific VariSoftTM...
The Issue: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClotTriever XL Catheter Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy system catheter instructions for use updated to reduce adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.