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

Recall Z-1752-2013 — ExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple sterile ingredients into a finished solution.

U.S. FDA — Device Enforcement · United States · 2013-06-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1752-2013
Date of alert: 2013-06-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Baxa Corporation
Product category: device
Product type: Devices

Reported risk: Baxter Healthcare is recalling certain ExactaMix automated compounding devices due to the complementary metal oxide semi-conductor battery failure resulting in resetting the internal clock of the device to midnight December 31, 2010.

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-1752-2013 — ExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple sterile ingredients into a finished solution.

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