DPS 1mlRecalls & reported problems
Jiangsu Shenli Medical Production Co.,Ltd. · DPS Bare Hypodermic Syringe,1ml Luer Lock,Needle not included · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06935550810011), received between Jun 14, 2022 and Jun 14, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incorrect Measurement” (1 report).
2 other recalls cover devices cleared under the same FDA submission (K103830); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Incorrect Measurement1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 14, 2022Incorrect Measurement; Incorrect Measurement
CUSTOMER REPORTED THAT THE SHAPE OF THE PLUNGER OF THE SYRINGE PROVIDED IN THE ANCILLARY CONVENIENCE KIT IS CAUSING AN INACCURATE MEASUREMENT OF VACCINE. THE CUSTOMER STATED THAT THEY MEASURED THE SYRINGES AGAINST OTHERS USED IN THE PAST AND CLAIM THAT THERE IS A DISPARITY IN THE ACCURACY OF THE DOSAGES. CUSTOMER STATED THAT WHILE DRAWING UP 6 DOSAGES, MEDICATION WAS STILL LEFT IN THE VIAL, FOR EXAMPLE THE DOSAGE SHOULD BE 0.3 BUT DUE TO THE EXTRA STOPPER PULL RESULTED IN A DOSAGE AMOUNT OF LESS THAN 0.3.
Patient problems: Insufficient Information
MAUDE report 14687707 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K103830. One submission often covers many models, so check the product and lot details in each record.
- Z-2940-2024 · Jul 24, 2024 · Open, ClassifiedMcKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
- Z-3033-2024 · Apr 8, 2024 · Open, ClassifiedMedline Convenience kits labeled as: 1) SYRINGE CNTRL 10ML RED L/L LP , Pack Number DYNJSYCPP10R ; 2) SYRINGE CNTRL 10ML YEL L/L LP , Pack Number DYNJSYCPP10Y ; 3) SYRINGE KIT
Other Syringe, Piston devices
- BD Luer-Lok 309657Becton, Dickinson And Company · Syringe, piston1,266 reports
- BD Luer-Lok 309653Becton, Dickinson And Company · Syringe, piston948 reports
- BD Luer-Lok 309628Becton, Dickinson And Company · Syringe, piston862 reports
- N/A 302995Becton, Dickinson And Company · Syringe, piston1 recall537 reports
- BD Plastipak Syringe 300865Becton, Dickinson And Company · Syringe, piston515 reports
- N/A 302830Becton, Dickinson And Company · Syringe, piston462 reports
- N/A 302832Becton, Dickinson And Company · Syringe, piston424 reports
- BD Ultra-Fine 328468Becton, Dickinson and Company Inc · Syringe, piston323 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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