Paramed Systems Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product 11-778-01. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product 11-778-01.
Brand
Paramed Systems
Lot Codes / Batch Numbers
Lot number 08/219/B.
Products Sold
Lot number 08/219/B.
Paramed Systems is recalling Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product due to Possible partial board disassembly due to inadequate webbing attachment.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possible partial board disassembly due to inadequate webbing attachment.
Recommended Action
Per FDA guidance
Customers were notified by letter and phone during 10/20/2008 and 10/29/2008 to schedule visits by Paramed to correct the devices.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026