(l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3)… — Class II medical device recall Z-0657-2013
Terminated recall by Stryker Communications, Inc., reported 2013-01-16, distributed nationwide. Stryker has become aware that there is a low likelihood of incomplete engagement of the Spring Arm Circlip dur
| Recall number | Z-0657-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Communications, Inc., Flower Mound, TX, United States |
| Recall initiated | 2012-09-25 |
| Classified | 2013-01-09 |
| Reported by FDA | 2013-01-16 |
| Terminated | 2013-04-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BR, CA, ES, FR, GB, HK, IN, JP, KR, MX, NL, NZ, PH, SG, TW |
Product
(l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat Panel and Navigation Arm The Spring Arm Circlip is part of the Stryker Spring Arm used in multiple configurations as a component of the (1)Visum Halogen Surgical Light, (2)Visum LED Surgical Light, and (3)Stryker Flat Panel and Navigation Arm. The Spring Arm that is subject to this field action suspends loads, is a conduit for power/data, and facilitates multi-directional movement. The Spring Arms that have been identified within scope are replacement parts that have potentially been serviced incorrectly.
Reason for recall
Stryker has become aware that there is a low likelihood of incomplete engagement of the Spring Arm Circlip during service or replacement of the Spring Arm. If the Spring Arm Circlip is not fully seated, the Spring Arm could separate and fall along with the surgical lights or monitors mounted to the end of the Spring Arm. To date, there have been no serious injuries reported from the incomplete e
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-0657-2013. 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.