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Terminated

Junction Box - 1104343 and 1193560

FDA Recall Z-1185-2017 · Posted None

Recalling FirmInvacare Corporation
Recall StatusTerminated
Product CodeLLI
Date Initiated2016-12-02
Date Terminated2017-11-02
Product Quantity161 units

Reason for Recall

A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.

Firm 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.

Root Cause

Component design/selection

Distribution Pattern

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

Official Source

View FDA Recall →

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

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