MedStream Programmable Infusion Pump — Class II medical device recall Z-1571-2014
Terminated recall by Codman & Shurtleff, Inc., reported 2014-05-21. A small number of specific pumps may trigger a low battery alarm at the beginning of the implanted life.
| Recall number | Z-1571-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Codman & Shurtleff, Inc., Raynham, MA, United States |
| Recall initiated | 2015-11-10 |
| Classified | 2014-05-09 |
| Reported by FDA | 2014-05-21 |
| Terminated | 2015-11-10 |
| Countries outside the US | BE, DE, ES, GB, IE, IT, RU, TR |
| Quantity | 90 |
Product
MedStream Programmable Infusion Pump, 20 mL, Product Code: 91-4200 The MedStream programmable pump is intended for the intrathecal delivery of Baclofen in the US market and for the intrathecal delivery of Morphine or Baclofen in the EMEA market.
Reason for recall
A small number of specific pumps may trigger a low battery alarm at the beginning of the implanted life.
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-1571-2014. 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.