FDA Device recall Z-2783-2016
Light Adaptor for Small Battery Drive and Small Battery Drive II
- FDA Device
- Class I
- terminated
- Published 2016-10-05
On 2016-10-05 the FDA classified a Class I recall of Light Adaptor for Small Battery Drive and Small Battery Drive II by The Anspach Effort, citing 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 b….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2783-2016 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-06-24 |
| Published | 2016-10-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | The Anspach Effort |
| Distribution | US |
Product
Light Adaptor for Small Battery Drive and Small Battery Drive II.
Reason
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.
Identifiers
| code_info | Model/Catalog: Part # (05.001.108 and 05.001.024) Serial: All Serial Numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2783-2016%22
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