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. 2,591 recalls have been distributed to Arkansas in the last 12 months.
Showing 15261–15280 of 49,990 recalls
Recalled Item: Clio Greek Yogurt Bar Strawberry Minis 6.2oz pouch x 6 Recalled by Clio LLC...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clio Greek Yogurt Bar Vanilla 50g x 10 Clio Retail Recalled by Clio LLC Due...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clio Greek Yogurt Bar Vanilla / Strawberry Club pack 50g x 12 Recalled by...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clio Yogurt Bar Strawberry 50g x 10 Clio Retail 10-pack. Code: 861703000113...
The Issue: Possible metal fragments in Yogurt Bars
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diflorasone Diacetate Ointment USP Recalled by Teligent Pharma, Inc. Due to...
The Issue: Presence of Foreign Substance: Foreign particles observed during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: READYPREP CHG Recalled by Medline Industries Inc Due to Superpotent Drug:...
The Issue: Superpotent Drug: Product is above specification for active ingredient, 2%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Recalled...
The Issue: Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX UNLTRperc Percutaneous Dilation Tracheostomy Kit Recalled by Smiths...
The Issue: One lot number of a specific model of ULTRAperc Percutaneous Dilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Angio Cath Removal Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirolimus Tablets 1 mg Recalled by American Health Packaging Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.