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 17921–17940 of 28,355 recalls
Recalled Item: 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable PICC Kit Catheter Recalled by Arrow International...
The Issue: The Arrow Pressure Injectable PICC is intended for short-term or long-term...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow MAC Two-Lumen Central Venous Access Kit Introducer Catheter The...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: Recalled by...
The Issue: Cotton tip of the device may disengage due to insufficient adhesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Correction...
The Issue: Correction to the product Instructions for Use because the current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...
The Issue: When cut lines are shown on an image, the lines may go from being vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Durability characteristics of reusable instruments were not established
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Merge PACS did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrophysiology catheter cables are designed as electrode cables with a...
The Issue: Sterilmed is recalling all lots of specific product codes of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beekley Medical 0-SPOT Mammography Skin Markers Recalled by Beekley...
The Issue: Mammography Skin Marker 0 -SPOT () product was mis-labeled with A-SPOT () labels
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Warmer System (IWS) Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.