Foot Section - BAR5490IVC recall
Foot Section - BAR5490IVC
Why was Foot Section - BAR5490IVC recalled?
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
BAR5490IVC
- Product
- Foot Section - BAR5490IVC
- Recalling firm
- Invacare Corporation
- Quantity
- 292 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
- Recall date
- February 15, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)