Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    DR SALMA'S SPINE DYNJ909111F UDI-DI 40198459130794 (case), 10198459130793 (ea) Lots 25FBE036 25GBV759; ORTHO SPINE FUMICH DYNJ901047R UDI-DI 40198459130466 (case), 10198459130465 (ea) Lots 25FBR230 25GBU693; PATTERSON TOTAL JOINT DYNJ909117G UDI-DI 40198459130480 (case), 10198459130489 (ea) Lots 25FBO307 25GBN625; TOTAL JOINT DYNJ902308K UDI-DI 40198459130596 (case), 10198459130595 (ea) Lots 25FBB321 25GBU688 KYPHOPLASTY DYNJ909113F UDI-DI 40198459130459 (case), 10198459130458 (ea) Lot 25IBM788
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Medline Industries, LP
Reason for Recall:
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT DYNJ909111F DR SALMA'S SPINE DYNJ909117G PATTERSON TOTAL JOINT DYNJ909113F KYPHOPLASTY

Product Codes/Lot Numbers:

DR SALMA'S SPINE DYNJ909111F UDI-DI 40198459130794 (case), 10198459130793 (ea) Lots 25FBE036 25GBV759; ORTHO SPINE FUMICH DYNJ901047R UDI-DI 40198459130466 (case), 10198459130465 (ea) Lots 25FBR230 25GBU693; PATTERSON TOTAL JOINT DYNJ909117G UDI-DI 40198459130480 (case), 10198459130489 (ea) Lots 25FBO307 25GBN625; TOTAL JOINT DYNJ902308K UDI-DI 40198459130596 (case), 10198459130595 (ea) Lots 25FBB321 25GBU688 KYPHOPLASTY DYNJ909113F UDI-DI 40198459130459 (case), 10198459130458 (ea) Lot 25IBM788

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0451-2026

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