SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Untreated, Blue Markings Model/Catalog Number: 06 0508 Product Description: A clear, plastic capillary blood collection tube
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model Number: 06 0508 GTIN : 30643351000384 UDI-DI: 10643351000380 All Lots produced from 1AUG2020 to 28FEB2025: 21F4062, 21L4388, 22G4487, 23C4341, 23F4164, 23G4172, 23G4210, 24I4053, 24I4327, 24I4330, 24I4331, 24I4409, 24J4141, 24J4350
- 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:
- ASP Global, LLC. dba Anatomy Supply Partners, LLC.
- Reason for Recall:
- Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
SAFE-T-FILL MicroHematocrit Capillary Tubes, 50 ¿L; Untreated, Blue Markings Model/Catalog Number: 06 0508 Product Description: A clear, plastic capillary blood collection tube
Product Codes/Lot Numbers:
Model Number: 06 0508 GTIN : 30643351000384 UDI-DI: 10643351000380 All Lots produced from 1AUG2020 to 28FEB2025: 21F4062, 21L4388, 22G4487, 23C4341, 23F4164, 23G4172, 23G4210, 24I4053, 24I4327, 24I4330, 24I4331, 24I4409, 24J4141, 24J4350
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0556-2026
Related Recalls
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.