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Terminated

Carroll Healthcare brand Arro bed models BA3180-151 AE, BA3180-151 PE, BA3180-151 FE, BA3180-171 AE, BA3180-171 FE and BA3180-171 FE.

FDA Recall Z-0919-05 · Posted 2005-06-22

Recalling FirmCarroll Healthcare Inc.
Recall StatusTerminated
Product CodeFNL
Date Initiated2005-05-17
Date Terminated2005-11-17

Reason for Recall

The diodes in the control panel may fail, which could result in the thermal breakdown of the circuit board inside of the control box, and cause the bed to cease functioning.

Firm Action

Consignees were sent a fax on 5/17/05 advising them of the problem and instructing them to lock-out the HILO pendant function on the attendant control pad until the firm visits their facility and corrects their beds.

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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