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

Recall Z-1138-2023 — NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)

U.S. FDA — Device Enforcement · United States · 2023-01-23 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1138-2023
Date of alert
2023-01-23
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Draeger Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04048675040552
Reported risk: The magnets used in the swivel frame/tube set and the headgear clips might impact medical devices (implanted as well as not implanted) and metallic implants.
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.