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. 2,502 recalls have been distributed to Arkansas in the last 12 months.
Showing 18621–18640 of 28,355 recalls
Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...
The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital...
The Issue: Digital templates were created with the incorrect files.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...
The Issue: A damaged temperature sensor at the endoscope's tip can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...
The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...
The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....
The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.