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. 1,852 recalls have been distributed to Alabama in the last 12 months.
Showing 28721–28740 of 50,591 recalls
Recalled Item: Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 Recalled by...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adenosine in 0.9% Sodium Chloride 30mL Recalled by Cantrell Drug Company Due...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Injection Solution Recalled by Cantrell Drug Company Due to...
The Issue: Lack of Sterility Assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine 40 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 60 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (as citrate) 10 mcg per mL in 0.9% Sodium Chloride 250 mL Bag...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2 mcg/mL + Ropivacaine 0.2% PF in NS 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine 200 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem 125 mg in 0.9% Sodium Chloride Recalled by SCA Pharmaceuticals Due...
The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 2 mcg/mL+Bupivacaine 0.0625% PF in 0.9% Sodium Chloride 250 mL...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (as citrate) 5 mcg/mL In 250 mL 0.9% Sodium Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPIVacaine HCl 0.125% In 250 mL 0.9% Sodium Chloride Bag Recalled by SCA...
The Issue: Lack of Assurance of Sterility; product has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TD60 Transmitter battery charger used with the BeneVision Central Station...
The Issue: A damaged circuit board in the battery charger can cause the battery to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba...
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyCareLink Patient Monitors. It is intended for used with a Recalled by...
The Issue: Patients monitored on two (2) or more implanted Medtronic heart devices in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyCareLink Smart Patient Monitors. It is intended for use with Recalled by...
The Issue: Patients monitored on two (2) or more implanted Medtronic heart devices in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series A3/A5 Anesthesia Delivery System Recalled by Mindray DS USA, Inc....
The Issue: A software issue may result in the previous settings being applied instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.