FDA recall record · openFDA

Cypress Medical Products LLC

4 FDA recalls on record (2024) — 4 device. 4 still ongoing.

Class I (most serious)

Class II

Class III

ongoing

How to read this. A recall count is not a quality verdict — large manufacturers recall more simply by volume, and a voluntary recall is the safety system working as intended. The signal to weight is the Class I count (the FDA's most-serious tier — reasonable probability of serious harm or death) and whether recalls are still ongoing. Most recalls are Class II/III. "Ongoing" reflects openFDA's last-published status — device recalls often stay marked ongoing long after they're resolved in practice; confirm current status at the FDA.

Most common reasons

Due to a classification error in our inventory management system, these medical devices were shipped to customers that d 2

Affected syringes lack FDA clearance. 1

The syringes that were inadvertently shipped from the Distribution Center. This product was on quarantine because FDA ha 1

Recalls

McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS) Class II 2024-07-24 BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025 Class II 2024-08-20 Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008 Class II 2024-08-20 General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Numbe Class II 2024-08-06

RECORDED — these are the FDA's published recall enforcement records (openFDA). Recalls are listed under the exact firm name as filed; a large manufacturer may also file under name variants, so this may not be the company's complete cross-variant record — confirm at the FDA recall database. This page informs and routes; it is not medical advice or a verdict on the company.

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