CLASS II ONGOING Device recall · Reported 4 Sep 2024 · FDA Enforcement Report
McKesson Syringe 60CC, Luer Lock Tip, Sterile recalled
Cypress Medical Products is recalling McKesson Syringe 60CC, Luer Lock Tip, Sterile, distributed nationwide in the US. The recall was initiated on 24 Jul 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-2940-2024
- FDA event ID
- 95041
- Recalling firm
- Cypress Medical Products, Richmond, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 24 Jul 2024
- FDA classified
- 29 Aug 2024
- Reported
- 4 Sep 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Syringes & Needles
Timeline
| 24 Jul 2024 | Recall initiated by company | |
| 29 Aug 2024 | Classified by FDA | +36 days |
| 4 Sep 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Affected syringes lack FDA clearance.
Product as listed by the FDA
McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
Where it was distributed
US distribution only. Domestic distribution nationwide.
Questions about this recall
Why was it recalled?
Affected syringes lack FDA clearance.
Which lots are affected?
All lots of the affected product 102-S60C, SYRINGE, LL 60CC which are within their expiration date, are being recalled. Products were manufactured within the last five years. Affected lots: All lots beginning with alpha characters CLN. UDI-DI (01)30612479170316
Where was it sold?
US distribution only. Domestic distribution nationwide.
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.
More recalls from Cypress Medical Products
All 11| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | General Purpose Syringe McKesson Luer Lock Tip Without Safety recalled | Cypress Medical Products | Other | Nationwide |
| Device | CLASS II | Acceava Respiratory Strep A, CLIA Waived recalled | Cypress Medical Products | Other | Nationwide |
| Device | CLASS II | BinaxNOW Respiratory Strep A Test Kit, CLIA Waived recalled | Cypress Medical Products | Other | Nationwide |
| Device | CLASS II | McKesson Lap Sponge, X-Ray Detectable 12"x 12" recalled | Cypress Medical Products | Sterility | VA |
| Device | CLASS III | McKesson Consult Diagnostic Immunochemical Fecal Occult recalled | Cypress Medical Products | Packaging Defects | 27 states |
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| Device | CLASS II | Brachytherapy Applicator Advanced Gynecological Applicator recalled | Elekta | Other | Nationwide |
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