FDA Medical Device Recalls (openFDA)
Carroll Healthcare Inc.: 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.
- Recall number
- Z-0919-05
- 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.
- Status
- Terminated
- Initiated
- 2005-05-17
- Posted
- 2005-06-22
- Terminated
- 2005-11-17
- Reason
- 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.
- 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.
- Quantity
- not on file
- Distribution
- Nationwide.
- Lot, serial or model codes
- 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.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNL
- Firm FEI
- 3002706498
- Firm city
- London
- Firm state
- Ontario
- Firm country
- Canada
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28