Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used w
FDA device recall Z-1306-2015 · posted 2015-03-20 · Terminated
Recall details
- Recalling firm
- Penner Mfg Inc
- Reason for recall
- If the patient sits on either wing, not squarely on the center section of the Stretcher Lift, tipping and injury to the operator or patient could result. The device manual was updated with an additional warning statement.
- Action taken
- Beginning on 1/30/2015, the recalling firm sent letters via certified mail to their customers informing them of the change to the stretcher manual along with a revised manual which incorporated those changes. For questions regarding this recall call 402-694-5003.
- Root cause
- Use error
- Status
- Terminated
- Product code
- MMP
- Quantity affected
- 158
- Distribution
- Worldwide Distribution - USA (nationwide) and Internationally to Canada.
- Date initiated
- 2015-01-30
- Date posted
- 2015-03-20
- Date terminated
- 2016-03-10
- Location
- Aurora, NE
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| COVER-ALL, DRAPE-IT-ALL, CHAIR SLEVE, X-RAY SLEEVE, HEADREST COVER (K962288) | Pinnacle Products, Inc. | 1997-01-30 |