The Anspach Effort, Inc. Recall: ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx
The Anspach Effort, Inc. Recall: ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: The Anspach Effort, Inc.; Product: ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx Only*** This device is intended to be used with Anspac
| Recalling firm | The Anspach Effort, Inc. |
|---|---|
| Product | ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx Only*** This device is intended to be used with Anspach Systems |
| Reason for recall | The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden. . |
| Recall initiated | 20121128 |
| Recall number | Z-1887-2014 |
| Category | device |
| State | FL |
| Country | United States |
$29/mo
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