IIR remote control JUPITER — Class II medical device recall Z-0923-2015
Terminated recall by Trumpf Medical Systems, Inc., reported 2015-01-14, distributed in AL, AZ, CA, CT, FL, GA, IL, KS…. Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged
| Recall number | Z-0923-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trumpf Medical Systems, Inc., Charleston, SC, United States |
| Recall initiated | 2014-12-03 |
| Classified | 2015-01-06 |
| Reported by FDA | 2015-01-14 |
| Terminated | 2016-08-23 |
| Distributed | AL, AZ, CA, CT, FL, GA, IL, KS, LA, MD, MI, MS, NC, NH, NJ, NY, OH, OK, PA, RI, SC, TX, VA, WA, WI |
| Countries outside the US | CA |
| Quantity | 3,303 all |
Product
IIR remote control JUPITER, Material no.4544120, Serial number: to (incl.) 102006720. Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre to the patient transfer system.
Reason for recall
Complaints have been reported of unintended movement occurring during surgical cases due to the use of damaged JUPITER remotes
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-0923-2015. 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.