🔍 RecallPedia

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO BRONCH PACK, Pack Number DYKE1355; b) ENDO BASIC KIT, Pack Number DYKE1356; c) ENDOSCOPY KIT, Pack Number DYKE1771C

Class I - Dangerous
🏥 Medical Devices Recalled: June 27, 2024 MEDLINE INDUSTRIES, LP - Northfield Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    a) DYKE1355: UDI/DI case 40889942274193, UDI/DI each 10889942274192; Lot Numbers: 23LBB043, 24BBJ327, 24CBS751; b) DYKE1356: UDI/DI case 40889942274186, UDI/DI each 10889942274185; Lot Numbers: 23LBD062, 24ABA646, 24BBJ328, 24CBG449, 24DBE106, 24EBG238; c) DYKE1771C: UDI/DI case 40195327331994, UDI/DI each 10195327331993; Lot Numbers: 24ABX292
  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 - Northfield
Reason for Recall:
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ENDO BRONCH PACK, Pack Number DYKE1355; b) ENDO BASIC KIT, Pack Number DYKE1356; c) ENDOSCOPY KIT, Pack Number DYKE1771C

Product Codes/Lot Numbers:

a) DYKE1355: UDI/DI case 40889942274193, UDI/DI each 10889942274192; Lot Numbers: 23LBB043, 24BBJ327, 24CBS751; b) DYKE1356: UDI/DI case 40889942274186, UDI/DI each 10889942274185; Lot Numbers: 23LBD062, 24ABA646, 24BBJ328, 24CBG449, 24DBE106, 24EBG238; c) DYKE1771C: UDI/DI case 40195327331994, UDI/DI each 10195327331993; Lot Numbers: 24ABX292

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3111-2024

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