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

Recall Z-1428-2023 — Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Reference Part Numbers C-PTISYJ-100-HC-G-EU-FLEX8.5 (G57725), C-PTISYJ-100-HC-G-NA-FLEX7.5 (G57720), C-PTISYJ-100-HC-G-NA-FLEX8.5 (G57721), C-PTISY-100-HC-G-NA-FLEX8.5 (G57717), C-PTISY-100-HC-G-NA-FLEX7.5 (G57716)

U.S. FDA — Device Enforcement · United States · 2023-04-07 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1428-2023
Date of alert: 2023-04-07
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Cook Incorporated
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00827002577251

Reported risk: There were reports from customers that the tracheostomy in the sets and trays is not making a secure connection with the 15mm cap and other 15mm circuit components and accessories. This resulted in an unsecure connection between the device connector and circuit components, cap, or accessories.

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.

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