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. 2,478 recalls have been distributed to Arkansas in the last 12 months.
Showing 21721–21740 of 28,355 recalls
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Combo Set Case The cases hold surgical instrumentation in Recalled by...
The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thinflap System Case The cases hold surgical instrumentation in place...
The Issue: The lids on implant caddies within P/N 17-5000 and 19-5000 could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...
The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...
The Issue: A software fix has been released to prevent automatic movement resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...
The Issue: Unexpected rate of postoperative fractures resulting in the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...
The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiographic Injector. Medrad Mark 7 Arterion Injection System Recalled by...
The Issue: Software Version SW 005.006_SH, resulted in the removal of purge enforcement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ferno iNX Wheeled Stretcher Recalled by Ferno-Washington Inc Due to Hole...
The Issue: Hole elongation in the telescoping load frame channel. A hole elongation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...
The Issue: Potential to improperly characterize tissue within the jaws, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 Recalled by Trilliant Surgical Ltd. Due to Gridlock screw driver bits...
The Issue: Gridlock screw driver bits for the Gridlock Plating System were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.