Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,466 recalls have been distributed to Wyoming in the last 12 months.
Showing 17901–17920 of 27,462 recalls
Recalled Item: Arrow Pressure Injectable PICC Kit The Arrow International Pressure...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable PICC Kit The Arrow International Pressure...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High...
The Issue: The large-bore two-lumen catheter permits venous access to the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow(R) VPS(R) Access Kit for use with 5 Fr. Peripherally Recalled by Arrow...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickFlash Radial Artery/Arterial Line Catheterization Kit The Arrow¿...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit. The MAC Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-Lumen Hemodialysis Catheterization Kit with Blue Flex Tip(R) Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIZA Vertebral Body Replacement Recalled by Eden Spine Europe SA Due to...
The Issue: Complaints that implants have been disassembled by surgeons because of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ Administration Set Recalled by Smiths Medical ASD Inc. Due to Smiths...
The Issue: Smiths Medical has become aware that the drawing on the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Estradiol II Recalled by BioMerieux SA Due to Fulvestrant cross reacts...
The Issue: Fulvestrant cross reacts with the VIDAS Estradiol II immunoassay and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ortho Basic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.