Brand Name: MEDLINE Product Name: SYR 3ML L/S Model/Catalog Number: 83083 Product Description: NON-Sterile syringes without needles for single use Component: No

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Code: LOT: 63721010004,63721020002,63721040002,63721050002,63721060001,63721070001,63721080001, 63721090001,63721110001,63721120001,63722010001,63722020003,63722030001,63722050006, 63722060001,63722070005,63722080002,63722090002,63722100003,63722120002,63723020001, 63723030001,63723060001,63723070001,63723090002,63723100003,63723120002
  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:
Jiangsu Shenli Medical Production Co., Ltd.
Reason for Recall:
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Brand Name: MEDLINE Product Name: SYR 3ML L/S Model/Catalog Number: 83083 Product Description: NON-Sterile syringes without needles for single use Component: No

Product Codes/Lot Numbers:

Lot Code: LOT: 63721010004,63721020002,63721040002,63721050002,63721060001,63721070001,63721080001, 63721090001,63721110001,63721120001,63722010001,63722020003,63722030001,63722050006, 63722060001,63722070005,63722080002,63722090002,63722100003,63722120002,63723020001, 63723030001,63723060001,63723070001,63723090002,63723100003,63723120002

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2048-2024

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