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

Recall Z-2038-2014 — PALL Medical Breathing Circuit Filter, REF BB50T and BB50T-BULK , Rx ONLY Single use, bi-directional bacterial/viral removal filter. The filters are individually packaged in a clear, plastic pouch with black writing - 50 per case, or in bulk packaged 100 filters/bag and two bags per shipper for

U.S. FDA — Device Enforcement · United States · 2014-06-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2038-2014
Date of alert: 2014-06-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Pall Corporation
Product category: device
Product type: Devices

Reported risk: Possible leak from the filter allowing a small of amount of air to be released from the junction between the filter end cap (flat side of the filter) and the filter housing connection.

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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