Light Adaptor for Small Battery Drive and Small Battery Drive II — Class I medical device recall Z-2783-2016
Terminated recall by The Anspach Effort, Inc., reported 2016-10-05, distributed nationwide. There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to
| Recall number | Z-2783-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Anspach Effort, Inc., Palm Beach Gardens, FL, United States |
| Recall initiated | 2016-06-24 |
| Classified | 2016-09-26 |
| Reported by FDA | 2016-10-05 |
| Terminated | 2018-06-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BR, CA, CH, CL, CN, CO, CR, CZ, DE, DK, ES, FI, FR, GB, HK, HU, ID, IE, IL, IN, IT, JO, JP, KR, KW, LK, MX, MY, NL, NO, NP, NZ, PL, PT, RO, RU, SA, SE, SG, SI, SK, TH, TR, TW, VN, ZA |
Product
Light Adaptor for Small Battery Drive and Small Battery Drive II.
Reason for recall
There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to generate excessive internal pressure that may cause the products to burst.
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-2783-2016. 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.