Z-0919-05

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

Name: Z-0919-05 Carroll Healthcare brand Arro bed models BA3180-151 AE, BA3180-151 PE, BA3180-151 FE, BA3180-171 AE...
Creator: Carroll Healthcare Inc.
Published: 2005-05-17
License: https://open.fda.gov/license/

Carroll Healthcare, Inc. / initiated 2005-05-17 / Terminated

FDA source

Carroll Healthcare Inc. began a recall of 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 on 2005-05-17. The reason FDA records is "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". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0919-05
Status: Terminated
Initiated: 2005-05-17
Posted: 2005-06-22
Terminated: 2005-11-17
Recalling firm: Carroll Healthcare, Inc.
Product: 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.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
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.
FDA root cause: Other
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.
Distribution: Nationwide.
Product codes and lots: Serial numbers 374061 through 374065, 374489 through 374519, 374521 through 374531, 375262, 376203 through 376211, 376229 through 376236, 376268 through 376284, 376698, 377647, 377648, 380181, 381593, 382244, 382373 through 382382, 383163 through 383166, 384390 through 384399, 386463 through 386468, 387057 through 387066, 387977 through 388004, 388039 through 388046, 388049 through 388063, 388153 through 388195, 388515 through 388527, 388529, 388679 through 388681, 388728 through 388735 and 389410 through 389414.

Product code FNL

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)