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Terminated

PediDyne AC-Powered Adjustable Hospital Beds

FDA Recall Z-0751-03 · Posted 2003-04-18

Recalling FirmKinetic Concepts, Inc
Recall StatusTerminated
Product CodeIOQ
Date Initiated2000-04-11
Date Terminated2003-12-16
Product Quantity244 units

Reason for Recall

Battery Failure/ Outgassing

Firm Action

Service centers were notified of the new battery maintenance policy on 4/11/2000 in a Technical Bulletin and again on 9/11/2000. Non-service center customers were notified by letter in October 2002.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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