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. 1,915 recalls have been distributed to Arkansas in the last 12 months.
Showing 23781–23800 of 49,990 recalls
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Feast Mode Flavors Garlic Beer Seasoning Recalled by Feast Mode Blending &...
The Issue: Feast Mode Garlic Beer Seasoning is mislabeled as "Gluten Free"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Levetiracetam in 0.54 % Sodium Chloride Injection 1 Recalled by Dr. Reddy's...
The Issue: Labeling: Label Error on Declared Strength; the pre-printed text on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing, LLC Due to...
The Issue: packaging error; An internal QA inspection revealed that a incorrect healing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: This recall has been initiated due to a possible leakage of a hose in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apple juice concentrate and organic apple juice concentrate in 52 gallon...
The Issue: The apple juice concentrates contain high levels of inorganic arsenic. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO...
The Issue: There is a potential for blood leakage at the blood inlet connector when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 20mm Compress Device Short Anchor Plug With Drill Set Recalled by...
The Issue: Potential metal burrs in the holes of the device preventing the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho-Novum 1/35 (norethindrone/ethinyl estradiol) Tablets Recalled by...
The Issue: Labeling: Incorrect Instructions; Instructions included for use with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortho-Novum 7/7/7 (norethindrone/ethinyl/estradiol) Tablets Recalled by...
The Issue: Labeling: Incorrect Instructions; Instructions included for use with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Catapres .2 (clonidine hydrochloride Recalled by Boehringer Ingelheim...
The Issue: Failed Dissolution Specifications: OOS resultsduring routine stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Essence Multi-slice CT Scanner System Product Usage: The Recalled...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 128 Multi-slice CT Scanner System Product Usage: The Multi-Slice...
The Issue: Software defect: For Helical scan with ClearView function, when small arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more...
The Issue: False resistant results for Streptococcus anginosus and Streptococcus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage:...
The Issue: Inspection process at the manufacturer found nonwoven material was used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.