Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1234-2017 — CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a BD 10cc LL Syringe, Sterile, Manufactured for CMS Custom Medical Specialties, Inc.

U.S. FDA — Device Enforcement · United States · 2016-09-20 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1234-2017
Date of alert: 2016-09-20
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Custom Medical Specialties, Inc.
Product category: device
Product type: Devices

Reported risk: Sterility of syringe product could not be assured.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1234-2017 — CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a BD 10cc LL Syringe, Sterile, Manufactured for CMS Custom Medical Specialties, Inc.

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