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

Recall Z-0487-2015 — Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose of infants to provide

U.S. FDA — Device Enforcement · United States · 2007-01-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0487-2015
Date of alert: 2007-01-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Beevers Manufacturing & Supply, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20060928

Reported risk: Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.

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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