ExactaMix 1200 and 2400 Compounders — Class II medical device recall Z-1752-2013
Terminated recall by Baxa Corporation, reported 2013-07-24, distributed nationwide. Baxter Healthcare is recalling certain ExactaMix automated compounding devices due to the complementary metal
| Recall number | Z-1752-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxa Corporation, Englewood, CO, United States |
| Recall initiated | 2013-06-04 |
| Classified | 2013-07-18 |
| Reported by FDA | 2013-07-24 |
| Terminated | 2015-10-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, TW |
| Quantity | 753 units |
| Serial numbers | 40005-40335, 45004-45481 |
Product
ExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple sterile ingredients into a finished solution.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1752-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.