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Lower risk Medical device recall · FDA · Published July 24, 2024

Cypress Medical Products Recalls 60CC Syringes Lacking FDA Clearance

Cypress Medical Products is recalling all 60CC syringes with model 102-S60C that lack FDA clearance. This may pose a risk of improper use. Consumers should check if their syringes start with lot code CLN.

🇺🇸 FDA recall #Z-2940-2024Medical deviceCypress Medical Products ›
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Recalling firmCypress Medical Products LLC9954 Mayland Dr · Richmond, VA 23233-1464
✎ GovInfoNow plain-language explainer

Cypress Medical Products is recalling all 60CC syringes with model number 102-S60C that lack FDA clearance. This means the syringes may not be safe for medical use as they were not approved by the FDA. Read more at govinfonow.com/recall/54560-cypress-medical-products-recalls-60cc-syringes-lacking-fda-clearance.

Source Summary by GovInfoNow · govinfonow.com/recall/54560-cypress-medical-products-recalls-60cc-syringes-lacking-fda-clearance · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2940-2024

Cite this page

“Cypress Medical Products Recalls 60CC Syringes Lacking FDA Clearance.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54560-cypress-medical-products-recalls-60cc-syringes-lacking-fda-clearance. Based on FDA recall #Z-2940-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2940-2024%22&limit=1).

The FDA announced on July 24, 2024, that Cypress Medical Products LLC is recalling McKesson Syringe 60CC units because they lack FDA clearance. The agency issued recall number Z-2940-2024 for the Class II voluntary recall.

How to tell if you have it

  • Brand: Cypress Medical Products
  • Product: McKesson Syringe 60CC, Luer Lock Tip, Sterile
  • Item No: 102-S60C
  • Model No: 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
  • UPC: 30612479170316
  • Lot codes: All lots beginning with alpha characters CLN
  • Quantity: 24,693,200 eaches

The hazard

The recalled syringes lack FDA clearance. The product was inadvertently shipped from the Distribution Center while on quarantine.

Context

GovInfoNow's records show Cypress Medical Products LLC has 7 other recalls on record since November 17, 2017. Other recent recalls include a August 6, 2024 recall of 60mL syringes lacking FDA clearance and an August 20, 2024 recall of Acceava Respiratory Strep A kits due to licensing errors. Similar recent recalls of unapproved syringes include Medline Convenience Kits recalled on February 27, 2026.

How to tell if you have this one

Check the syringe model number for 102-S60C. Affected lots begin with the alpha characters CLN. The syringes were manufactured within the last five years.

  • Brand
    Cypress Medical Products
  • Product
    McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Model Number

    Look for the model number 102-S60C on the syringe packaging or label.

  2. Verify Lot Code

    Ensure the lot code starts with the letters CLN to confirm it is affected.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US distribution only. Domestic distribution nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: Jul 24, 202412. FDA classified it Class II: Aug 29, 202423. Published in FDA’s Enforcement Report: Sep 4, 202432024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-2940-2024 (July 24, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2940-2024 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA