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

Recall Z-1146-2017 — Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with 15mm O.D./I.D. Connections, Reference no. 1543A. The 15 mm Dual Spray MiniSpacer with Counter Incrementing Actuator is a non-sterile, single-use item, intended to dispense aerosolized medication into a breathing circuit or

U.S. FDA — Device Enforcement · United States · 2016-09-29 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1146-2017
Date of alert: 2016-09-29
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Thayer Medical Corporation
Product category: device
Product type: Devices

Reported risk: The insert and case label description of the device incorrectly reads Counter Incrementing Actuator with 22mm O.D./I.D. Connections.

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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