Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,661 recalls have been distributed to Arkansas in the last 12 months.
Showing 2841–2860 of 49,990 recalls
Recalled Item: Sofosbuvir and Velpatasvir Recalled by ASEGUA THERAPEUTICS LLC Due to...
The Issue: Defective Container: blister packs not properly sealed resulting in tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Super-Potent Drug: Out of specification potency results were obtained.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets 60 mg Recalled by Slate Run Pharmaceuticals...
The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Super-Potent Drug: Out of specification potency results were obtained.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets 30 mg Recalled by Slate Run Pharmaceuticals...
The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...
The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne...
The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...
The Issue: Chemical Contamination: This recall has been initiated due to detected trace...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRASUGREL TABLETS Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...
The Issue: Presence of foreign substance: Presence of Benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.