CLASS II ONGOING Device recall · Reported 25 Sep 2024 · FDA Enforcement Report
General Purpose Syringe McKesson Luer Lock Tip Without Safety recalled
Cypress Medical Products is recalling General Purpose Syringe McKesson Luer Lock Tip Without Safety, distributed nationwide in the US. The recall was initiated on 6 Aug 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-3154-2024
- FDA event ID
- 95223
- Recalling firm
- Cypress Medical Products, Richmond, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 6 Aug 2024
- FDA classified
- 16 Sep 2024
- Reported
- 25 Sep 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Syringes & Needles
Timeline
| 6 Aug 2024 | Recall initiated by company | |
| 16 Sep 2024 | Classified by FDA | +41 days |
| 25 Sep 2024 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
Product as listed by the FDA
General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Number: 102-S60C
Where it was distributed
US Nationwide distribution in the states of CA, NV, NY.
Questions about this recall
Why was it recalled?
The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA has stated that these syringes lack FDA clearance and were inadvertently shipped due to an internal order processing error.
Which lots are affected?
UDI-DI: 20612479170302;
Where was it sold?
US Nationwide distribution in the states of CA, NV, NY.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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