McKesson 102-SN1C2905PRecalls & reported problems
Mckesson Medical-Surgical Inc. · Insulin SYRINGE 1CC 29GX1/2" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20612479187881), received between Jul 23, 2024 and Aug 3, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
8 other recalls cover devices cleared under the same FDA submission (K151949, K993017); 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Insufficient Device Problem Information1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 3, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
NEEDLE BROKE OFF FROM SYRINGE/HUB WHILE IN USE ON A PATIENT. REQUIRED FORCEPS TO RETRIEVE NEEDLE FROM PATIENT SKIN. NOTED SKIN IRRITATION, POST RETRIAL. HAPPENED MORE THAN ONCE. FROM SEPARATE BOXES WITH SAME LOT#.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19901176 ↗InjuryJul 23, 2024Break; Break
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLE BROKE OFF FROM THE SYRINGE/HUB WHILE IN USE ON A PATIENT. FORCEPS WERE REQUIRED TO RETRIEVE THE NEEDLE FROM THE PATIENT'S SKIN. THERE WAS NOTED SKIN IRRITATION POST RETRIEVAL. THIS WAS REPORTED TO HAVE HAPPENED MORE THAN ONCE FROM SEPARATE BOXES WITH THE SAME LOT NUMBER.
Patient problems: Foreign Body In Patient; Skin Inflammation/ Irritation
MAUDE report 19804308 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K151949, K993017. One submission often covers many models, so check the product and lot details in each record.
- Z-0119-2019 · Sep 4, 2018 · TerminatedMcKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P Product Usage: Indication of Use: Injection of U-100 insulin only.
- Z-3202-2018 · Aug 24, 2018 · TerminatedDisposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are packaged in a flexible plastic (poly bag) and 10 flexible plastic (poly b
- Z-0569-2010 · Oct 27, 2009 · TerminatedAccuSure, U-100 28 Gauge, 1/2cc Insulin Syringe, 1/2" Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-6995-21. The device is intended to b
- Z-0574-2010 · Oct 27, 2009 · TerminatedAccuSure, U-100 30 Gauge, 1cc Insulin Syringe, 5/16" (8mm) Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-7000-21
- Z-0572-2010 · Oct 27, 2009 · TerminatedAccuSure, U-100 29 Gauge, 1cc Insulin Syringe, 1/2" Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-6998-21
- Z-0573-2010 · Oct 27, 2009 · TerminatedAccuSure, U-100 30 Gauge, 1/2cc Insulin Syringe, 5/16" (8mm) Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-6999-21
- Z-0571-2010 · Oct 27, 2009 · TerminatedAccuSure, U-100 29 Gauge, 1/2cc Insulin Syringe, 1/2" Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-6997-21
- Z-0570-2010 · Oct 27, 2009 · TerminatedAccuSure, U-100 28 Gauge, 1cc Insulin Syringe, 1/2" Needles, Short Needle, packaged 10 syringes per package, 10 packages per carton, NDC 0603-6996-21
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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