Recall Z-0568-2010
Paramed Systems · initiated October 29, 2008
Product
Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product 11-778-01.
Codes / lots: Lot number 08/219/B.
Reason for recall
Possible partial board disassembly due to inadequate webbing attachment.
FDA-determined cause: Process change control
Action taken
Customers were notified by letter and phone during 10/20/2008 and 10/29/2008 to schedule visits by Paramed to correct the devices.
Details
- Recall number
- Z-0568-2010
- Initiated
- October 29, 2008
- Posted by FDA
- December 28, 2009
- Terminated
- January 28, 2010
- Product code
- FPP – Stretcher, Hand-Carried
- Quantity
- 722 Units
- Distribution
- Nationwide Distribution -- Including states of AZ, CA, FL, GA, IL, IN, KS, KY, MA, MI, MT, NY, PA, SC, TN and UT.
- Recalling firm
- Paramed Systems, West Jordan, UT