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. 2,467 recalls have been distributed to Arkansas in the last 12 months.
Showing 22101–22120 of 28,355 recalls
Recalled Item: 3.2 mm Cannulated Drill Bit/ QC 170 mm 2.7 Cannulated Recalled by Synthes,...
The Issue: affected parts and lots of the Cannulated Drill Bits have the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws Recalled...
The Issue: Certain lots of the 3.7mm Cannulated Locking Screws and 3.7mm Cannulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Recalled by CareFusion 303, Inc. Due to An issue...
The Issue: An issue with the cancel functionality used during atypical infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite Analyser Recalled by The Binding Site Group, Ltd. Due to Potential...
The Issue: Potential risk of the Optilite lid/cover falling suddenly and causing injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEDASYS Computer-Assisted Personalized Sedation System Recalled by Ethicon...
The Issue: Ethicon has found that disinfecting methods not specified in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReUnion TSA Shoulder System Recalled by Stryker Howmedica Osteonics Corp....
The Issue: A package labeled as Part #5901-S-4818, Lot MAC7C14, standard humeral head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN Recalled by...
The Issue: There is a possibility that the thumb button remains in the depressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 208V Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alkaline Wash Recalled by Abbott Laboratories Due to The product is leaking...
The Issue: The product is leaking from the cap and crystallization was noted as present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 220-230V Recalled by...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...
The Issue: Potential lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...
The Issue: Potential lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Fast Absorbing Plain Gut - MultiPass Needles Recalled by Ethicon,...
The Issue: Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...
The Issue: Potential sterility breach in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.