MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI: 15051684022996 UPN: H965457561 Lot Number: 5796084 5796085 5796086 5796087 5796088 5796089 5796090 5796659 5796660 5796661 5796662 5796663 5796666 5797456 5797465 5798836 5798841 5798842 5799620 5800404 5803526 5804396
- 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:
- Angiodynamics, Inc.
- Reason for Recall:
- Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
Product Codes/Lot Numbers:
UDI: 15051684022996 UPN: H965457561 Lot Number: 5796084 5796085 5796086 5796087 5796088 5796089 5796090 5796659 5796660 5796661 5796662 5796663 5796666 5797456 5797465 5798836 5798841 5798842 5799620 5800404 5803526 5804396
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1339-2024
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