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

Recall Z-1033-2023 — Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case

U.S. FDA — Device Enforcement · United States · 2022-11-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1033-2023
Date of alert
2022-11-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
40195327029570
Reported risk: Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging.
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.

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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.