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

Medline CHEST TUBE REORDER NO: DYNJ36762A — recall Z-1683-2022

U.S. FDA — Device Enforcement · United States · 2022-07-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1683-2022
Date of alert
2022-07-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medline Industries Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
1019348989440
Reported risk: Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.

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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.