Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50 pouches per case
Class I - DangerousWhat Should You Do?
- Check if you have this product: Product Code: 142560488, Lot number (UDI Number): 865455H (20887787005237, 10887787005230), 896215H (20887787005237, 10887787005230), 897455H (20887787005237, 10887787005230), 3864785 (20887787005237, 10887787005230), 4095291 (20887787005237, 10887787005230);
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- ICU Medical Inc
- Reason for Recall:
- Potential for fluid leakage out of air vents on inline filters on Plum and Sapphire micropore infusion sets.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50 pouches per case
Product Codes/Lot Numbers:
Product Code: 142560488, Lot number (UDI Number): 865455H (20887787005237, 10887787005230), 896215H (20887787005237, 10887787005230), 897455H (20887787005237, 10887787005230), 3864785 (20887787005237, 10887787005230), 4095291 (20887787005237, 10887787005230);
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0127-2020
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