Junction Box - 1104343 and 1193560
Reported: February 15, 2017 Initiated: December 2, 2016 #Z-1185-2017
Product Description
Junction Box - 1104343 and 1193560
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.
Details
- Recalling Firm
- Invacare Corporation
- Units Affected
- 161 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
- Location
- Elyria, OH
Frequently Asked Questions
What product was recalled? ▼
Junction Box - 1104343 and 1193560. Recalled by Invacare Corporation. Units affected: 161 units.
Why was this product recalled? ▼
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 15, 2017. Severity: Moderate. Recall number: Z-1185-2017.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11