FDA Device recall Z-2047-2024
Brand Name: MEDLINE Product Name: SYR 10ML L/L Model/Catalog Number: 83082 Product Description: NON-Sterile syringes without needles for si…
- FDA Device
- Class II
- ongoing
- Published 2024-05-29
On 2024-05-29 the FDA classified a Class II recall of Brand Name: MEDLINE Product Name: SYR 10ML L/L Model/Catalog Number: 83082 Product Description: NON-Sterile syringes without needles for si… by Jiangsu Shenli Medical Production, citing piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2047-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-05 |
| Published | 2024-05-29 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Jiangsu Shenli Medical Production |
| Distribution | US |
Product
Brand Name: MEDLINE Product Name: SYR 10ML L/L Model/Catalog Number: 83082 Product Description: NON-Sterile syringes without needles for single use Component: No
Reason
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Identifiers
| code_info | Lot Code: LOT: 63721010001,63721010003,63721010004,63721040002,63721050002,63721060001,63721060002, 63721070001,6372107…Lot Code: LOT: 63721010001,63721010003,63721010004,63721040002,63721050002,63721060001,63721060002, 63721070001,63721070002,63721070003,63721070004,63721070006,63721080001,63721080002, 63721080003,63721080004,63721080005,63721090002,63721090003,63721090004,63721100001, 63721100002,63721100003,63721100004,63721100005,63722030001,63722030002,63722030004, 63722040001,63722040003,63722040006,63722050001,63722050002,63722050005,63722060001, 63722060002,63722060003,63722070002,63722070003,63722070004,63722070006,63722080002, 63722080004,63722080005,63722080007,63722090002,63722090004,63722090005,63722090006, 63722120002,63723010002,63723020001,63723020003,63723030001,63723050001,63723050002, 63723050003,63723060001,63723060002,63723070001,63723070002,63723070003,63723080001, 63723080002,63723080003,63723090002,63723090003,63723090004,63723100003,63723100004, 63723100006,63723100008,63723110002,63723110003,63723110005,63723120002,63723120003, 63723120004,63723120005,63723120006 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2047-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.