FDA Medical Device Recalls (openFDA)
Invacare Corporation: Bariatric Bed - BAR600IVC
- Recall number
- Z-1182-2017
- Recalling firm
- Invacare Corporation
- Product
- Bariatric Bed - BAR600IVC
- Status
- Terminated
- Initiated
- 2016-12-02
- Posted
- not on file
- Terminated
- 2017-11-02
- Reason
- The junction box used in the bariatric bed may emit sparks and result in a fire.
- Root cause
- Component design/selection
- Action
- All customers were notified via letter with return receipt. This notification will include a provider letter, provider response card, impacted unit list and a consumer letter. Consignees will be instructed conduct sub-recalls as necessary. Follow-up telephone calls will be made to nonresponders.
- Quantity
- 411 Units
- Distribution
- Products were distributed in the following states: AK, AL, AR, CA, CO, CT, FL, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI. No foreign accounts
- Lot, serial or model codes
- BAR600IVC
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LLI
- Firm FEI
- 3002889431
- Firm city
- Elyria
- Firm state
- OH
- Firm country
- not on file
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