Medline convenience kits containing semi-rigid suction liners labeled as follows: a) MINOR BREAST, Pack Number DYNJ908104B; b) PLASTIC MAJOR, Pack Number DYNJ908106B; c) ABDOMINOPLASTY W/LIPO SUCTION, Pack Number DYNJ909946; d) PLASTIC, Pack Number DYNJ909951
Class I - DangerousWhat Should You Do?
- Check if you have this product: a) DYNJ908104B: UDI/DI case 40195327507115, UDI/DI each 10195327507114, Lot Numbers: 23LBT869, 24BBQ730; b) DYNJ908106B: UDI/DI case 40195327507139, UDI/DI each 10195327507138, Lot Numbers: 24ABB087, 24CBM739, 24EBH234; c) DYNJ909946: UDI/DI case 40195327512652, UDI/DI each 10195327512651, Lot Numbers: 23LBD934, 24DBB806; d) DYNJ909951: UDI/DI case 40195327512904, UDI/DI each 10195327512903, Lot Numbers: 23LBD932, 24ABP740
- 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:
- 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) MINOR BREAST, Pack Number DYNJ908104B; b) PLASTIC MAJOR, Pack Number DYNJ908106B; c) ABDOMINOPLASTY W/LIPO SUCTION, Pack Number DYNJ909946; d) PLASTIC, Pack Number DYNJ909951
Product Codes/Lot Numbers:
a) DYNJ908104B: UDI/DI case 40195327507115, UDI/DI each 10195327507114, Lot Numbers: 23LBT869, 24BBQ730; b) DYNJ908106B: UDI/DI case 40195327507139, UDI/DI each 10195327507138, Lot Numbers: 24ABB087, 24CBM739, 24EBH234; c) DYNJ909946: UDI/DI case 40195327512652, UDI/DI each 10195327512651, Lot Numbers: 23LBD934, 24DBB806; d) DYNJ909951: UDI/DI case 40195327512904, UDI/DI each 10195327512903, Lot Numbers: 23LBD932, 24ABP740
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-3113-2024
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