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. 2,491 recalls have been distributed to Arkansas in the last 12 months.
Showing 19181–19200 of 28,355 recalls
Recalled Item: 6.5CM ADLT CRANI Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otologic Curved Micro Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.0cm Medium Attachment Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRI SHORT HD ATTACHMENT Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.9CM ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AL-III W/ male disconnect and 20ft hose Product Usage: Pneumatic system...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bearing Sleeve Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC CRANIOTOME Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III Product Usage: Pneumatic system Recalled by The Anspach Effort,...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory Adapter Part number 600525A0 Product Usage: designed for the...
The Issue: Maquet Inc. is initiating a voluntary field action on the Accessory Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm Recalled...
The Issue: The Drager Pendula spring arm device has a set of screws located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alligator Retrieval Device The device is intended for use in Recalled by...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...
The Issue: The device defect is a positive bias of up to 20% relative to the currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.