Recall record at a glance
| Official record | 94520 |
|---|---|
| Category | Medical Device Recalls |
| Classification | Not Yet Classified |
| FDA record status | Ongoing |
| Recalling firm | Jiangsu Shenli Medical Production Co., Ltd. |
| Report date | May 29, 2024 |
| Recall initiation date | Apr 5, 2024 |
| Quantity | 4092250 |
| Location | Changzhou, China |
Official product description
Brand Name: MEDLINE Product Name: SYR 30ML L/L Model/Catalog Number: 83078 Product Description: NON-Sterile syringes without needles for single use Component: No
Why the product was recalled
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Distribution information
U.S.: CA, FL, GA, IL, TN, and VA After customers place US orders, then arrange production, then deliver to the cargos to customer designated port or warehouse, mostly in Shanghai port. The shipping company will ship the cargos to different destination such as Chicago, Los Angeles, Long beach, Miami, Savannah, Nashville, and Norfolk.
How to read the classification
The classification “Not Yet Classified” is reproduced from the official source record. Refer to the FDA record for the agency’s current classification and instructions.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.