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Terminated

Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product 11-778-01.

FDA Recall Z-0568-2010 · Posted 2009-12-28

Recalling FirmParamed Systems
Recall StatusTerminated
Product CodeFPP
Date Initiated2008-10-29
Date Terminated2010-01-28
Product Quantity722 Units

Reason for Recall

Possible partial board disassembly due to inadequate webbing attachment.

Firm Action

Customers were notified by letter and phone during 10/20/2008 and 10/29/2008 to schedule visits by Paramed to correct the devices.

Root Cause

Process change control

Distribution Pattern

Nationwide Distribution -- Including states of AZ, CA, FL, GA, IL, IN, KS, KY, MA, MI, MT, NY, PA, SC, TN and UT.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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