Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported May 29, 2024
Brand Name: MEDLINE Product Name: SYR 10ML L/L YELLOW Model/Catalog Number: 91834 Product Description: NON-Sterile syringes without needles for single use Component: No
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Jiangsu Shenli Medical Production Co., Ltd. recalled Brand Name: MEDLINE Product Name: SYR 10ML L/L YELLOW Model/Catalog Number: 91834 Prod… - a moderate-severity action.
Brand Name: MEDLINE Product Name: SYR 10ML L/L YELLOW Model/Catalog Number: 91834 Prod… was recalled by Jiangsu Shenli Medical Production Co., Ltd. in May 29, 2024. Reason: Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).. Check the official notice for the remedy. Verify recall #Z-2066-2024 with the FDA Devices before acting.
The recall
Jiangsu Shenli Medical Production Co., Ltd. issued this moderate-severity FDA Devices recall — Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k)..
- Moderate
- severity level
- 749K units
- affected scope
- Class II
- classification
- May 29, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2066-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2066-2024) was formally reported on May 29, 2024, with the manufacturer initiating the action on April 5, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Jiangsu Shenli Medical Production Co., Ltd. is listed as the recalling firm, operating out of Changzhou. Federal records list the affected scope as 749400, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k). Distribution data in the federal record shows the product reached: U.S. Nationwide distribution in the states of 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 Shangh…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category — 40,409 medical devices recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
749400
Related Recalls
6
6 from same agency
Product description
Brand Name: MEDLINE Product Name: SYR 10ML L/L YELLOW Model/Catalog Number: 91834 Product Description: NON-Sterile syringes without needles for single use Component: No
Reason for recall
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2066-2024 |
| Date reported | May 29, 2024 |
| Date initiated | April 5, 2024 |
| Recalling firm | Jiangsu Shenli Medical Production Co., Ltd. |
| Firm location | Changzhou |
| Affected scope | 749400 |
| Distribution | U.S. Nationwide distribution in the states of 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 shippin… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2066-2024) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting — recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Brand Name: MEDLINE Product Name: SYR 10ML L/L YELLOW Model/Catalog Number: 91834 Product Description: NON-Sterile syringes without needles for single use Component: No. Recalled by Jiangsu Shenli Medical Production Co., Ltd.. Units affected: 749400.
Why was this product recalled? ▼
Piston syringes sizes and configurations are out of the range of devices cleared under the firm's 510(k).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 29, 2024. Severity: Moderate. Recall number: Z-2066-2024.
Where was the recalled product distributed? ▼
Distribution: U.S. Nationwide distribution in the states of 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 do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2066-2024) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Devices, reported May 29, 2024.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.