Lower riskMedical device recall · FDA · Published August 6, 2024
Cypress Medical: 60mL Syringes Lacking FDA Clearance - Recall
Cypress Medical recalls 60mL syringes (Catalog 869662) that were inadvertently shipped without FDA clearance due to an internal order error. No action needed as they are on quarantine.
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.
Take action
Contact the company
📍Recalling firmCypress Medical Products LLC9954 Mayland Dr · Richmond, VA 23233-1464
✎ GovInfoNow plain-language explainer
Cypress Medical is recalling 60mL syringes with catalog number 869662 that were shipped without FDA clearance. These syringes are on quarantine and no action is required as they were inadvertently shipped due to an internal order processing error. Read more at govinfonow.com/recall/54308-cypress-medical-60ml-syringes-lacking-fda-clearance-recall.
“Cypress Medical: 60mL Syringes Lacking FDA Clearance - Recall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54308-cypress-medical-60ml-syringes-lacking-fda-clearance-recall. Based on FDA recall #Z-3154-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3154-2024%22&limit=1).
The FDA announced on Aug. 6, 2024, that Cypress Medical Products LLC is recalling General Purpose Syringes because they lack FDA clearance. The agency stated the devices were inadvertently shipped due to an internal order processing error.
How to tell if you have it
Brand: McKesson
Product: General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety
Catalog Number (Cypress): 869662
Catalog Number (McKesson): 102-S60C
UDI-DI: 20612479170302
The hazard
The FDA stated that the recalled syringes lack FDA clearance. The products were shipped from a distribution center due to an internal order processing error.
Context
GovInfoNow's records show Cypress Medical Products LLC has issued seven other recalls since Nov. 17, 2017. Other recent recalls of similar products include Medline Syringes Recall: 510(k) Clearances Rescinded for Safety (Feb. 25, 2026), Medline Control Syringes Recalled: 510(k) Clearances Rescinded (Feb. 25, 2026), and Medline Convenience Kits with Unapproved Syringes Recalled (Feb. 27, 2026).
How to tell if you have this one
Check for catalog number 869662 on the syringe packaging. These syringes were shipped by Cypress Medical under the McKesson brand.
Brand
Cypress Medical
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Syringe Packaging
Look for catalog number 869662 on the syringe packaging or label.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 3 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of CA, NV, NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Nevada, New York.
Recall timeline
FDA published this recall 50 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-3154-2024 (August 6, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3154-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.