McKesson 306609Recalls & reported problems
Mckesson Medical-Surgical Inc. · Safety Hypodermic Needles GLIDE Thin Wall 25G x 5/8 in (50/bx, 10/cs) · Class 2
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10612479262567), received between Jun 27, 2023 and Jun 10, 2025 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Break” (4 reports).
4 other recalls cover devices cleared under the same FDA submission (K951254); 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break4
- Complete Blockage1
- Detachment of Device or Device Component1
- Partial Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 10, 2025Break; Break
IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 25X5/8 RB MCK NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 306609, BATCH#: 5016206 & 4054382. RCC RECEIVED A COMPLAINT VIA EMAIL. WHILE DRAWING UP MEDICATION FROM VIAL, NEEDLE DETACHED FROM SYRINGE AND REMAINED STUCK IN MEDICATION. PRODUCT NAME: NEEDLE, SFTY 192-N2558S PREVENT SG ORG 25GX5/8", LOT / SERIAL NUMBER (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22178924 ↗MalfunctionJun 10, 2025Break; Break
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22178919 ↗MalfunctionMay 30, 2025Break; Break
IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 25X5/8 RB MCK NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 306609 BATCH # 5016206. RCC RECEIVED A COMPLAINT VIA EMAIL. COMPLAINT NUMBER (B)(4), REPORT DATE (B)(6) 2025, FACTORY/MANUFACTURER BD, MFR REORDER # 192-N2558S, PRODUCT NAME - NEEDLE, SFTY 192-N2558S PREVENT SG ORG 25GX5/8". NEEDLE DETACHED FROM HUB AND WAS LEFT IN PATIENT. WE HAD AN INCIDENT WITH A NEEDLE YESTERDAY. A BABY WAS GIVEN A VACCINE AND WHEN THE NURSE PULLED BACK THE NEEDLE, THE NEEDLE STAYED IN THE BABY¿S LEG COMPLETELY DISCONNECTED FROM THE SYRINGE. THANKFULLY THE NURSE WAS ABLE TO REMOVE THE NEEDLE WITH TWEEZERS SO NO INJURY WAS NOTED FOR THE CHILD. THE NEEDLES /SYRINGE IS LOT # 5016206. WE HAVE CURRENTLY 10 BOXES OF THIS LOT THAT I HAD STAFF PULL. I HAVE INCLUDED THE IMAGE ADDITIONAL INFORMATION PROVIDED: 1. KINDLY PROVIDE THE DATE OF EVENT. 08 MAY 2025. 2. DESCRIBE ANY PATIENT HARM, INJURY, COMPLICATION OR NEGATIVE OUTCOME THAT OCCURRED AS A RESULT OF THE EVENT NEGATIVE OUTCOME - SLOWED DOWN OUR PRODUCTION. - NO INJURIES NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22119027 ↗MalfunctionApr 15, 2025Break; Break
IT WAS REPORTED THAT THE BD NEEDLE SFTYGLD 25X5/8 RB MCK NEEDLE WAS BROKEN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL #306609, LOT # UNKNOWN. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. COMPLAINT NUMBER: (B)(4). REPORT DATE: 03.28.25. FACTORY/MANUFACTURER: BD. MFR REORDER #: (B)(4). PRODUCT NAME: NEEDLE, SFTY 192-N2558S PREVENT SG ORG 25GX5/8". LOT / SERIAL NUMBER: UNKNOWN. PRODUCT CONCERN: NEEDLE SNAPPED OFF WHEN ACTIVATED THE SAFETY MECHANISM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21845527 ↗MalfunctionOct 10, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17909094 ↗MalfunctionJul 6, 2023Partial Blockage; Partial Blockage
IT WAS REPORTED WHILE USING BD SAFETYGLIDE¿ NEEDLE ONLY THE NEEDLE WAS CLOGGED. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER REPORTED TEAM MEMBER ADMINISTERED VACCINE SUBCUTANEOUSLY IN RIGHT THIGH. ADMINISTRATION OF VACCINE WAS COMPLICATED BY THE NEED FOR ADDITIONAL FORCE ON THE PLUNGER REQUIRED TO INJECT MEDICATION-TEAM MEMBER REPORTS THAT THE NEEDLE FELT BLOCKED. FULL DOSE OF MEDICATION WAS ADMINISTERED OVER LONGER THAN USUAL TIME. NO HARM TO PATIENT- NO EXTRA INJECTION REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17276165 ↗MalfunctionJun 27, 2023Complete Blockage; Complete Blockage
IT WAS REPORTED WHILE USING BD SAFETYGLIDE NEEDLE THE NEEDLE WAS BLOCKED. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: VERY DIFFICULT TO PUSH THE VACCINE THROUGH THE NEEDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17211311 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K951254. One submission often covers many models, so check the product and lot details in each record.
- Z-2889-2020 · Jul 28, 2020 · TerminatedBD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
- Z-0315-2018 · Jul 5, 2017 · TerminatedSafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion component code BD17O1NS.
- Z-3116-2017 · Jun 13, 2017 · TerminatedBD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose injection, aspiration of fluids from
- Z-2748-2017 · Sep 16, 2016 · TerminatedBD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle is intended to be used for general purpose injection, aspiration of fluids from parts of the body below th
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.