[Recalled] Keyless Driver Product Usage: Pneumatic system — Supplied Directions for Use (DFU) did not contain a recommended service interval | FDA 2016-10-06
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Keyless Driver Product Usage: Pneumatic system |
|---|---|
| Brand / manufacturer | The Anspach Effort, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1995-2017 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 October 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Supplied Directions for Use (DFU) did not contain a recommended service interval.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from The Anspach Effort, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.