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

Recall Z-1442-2020 — BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The BodyGuard Infusion Pump System is designed to transfer medication and fluids intravenously.

U.S. FDA — Device Enforcement · United States · 2019-09-16 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1442-2020
Date of alert: 2019-09-16
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: CME America, LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00818666020146

Reported risk: When using a specific tubing set with infusion pump system, may result in under deliver of fluids.

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.

Recall Z-1442-2020 — BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The BodyGuard Infusion Pump System is designed to transfer medication and fluids intravenously.

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