Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,859 recalls have been distributed to Iowa in the last 12 months.
Showing 26401–26420 of 49,990 recalls
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extension Line Slide Clamps Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLock" Catheter/Syringe Adapter Recalled by Arrow International Inc Due...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural Needle Recalled by Arrow International Inc Due to Product sterility...
The Issue: Product sterility may be compromised due to unsealed 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: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Arterial Access Kit Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate2 Balloon Guide Catheter Recalled by Stryker Neurovascular Due to...
The Issue: There may be product manufactured with the outer diameter of the balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Multi-Lumen CVC Kit Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
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: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peel Away Sheath over Dilator Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.