Invacare Recalls Bariatric Beds Due to Fire Hazard
Invacare is recalling Bariatric Beds (BARPKG-IVC 1633) because a quality issue with the junction box may cause sparks and result in a fire.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall involves a fire hazard, which is a significant injury/property-damage risk. Per the rubric, significant injury/property-damage reports or risks warrant a score of 4 (Severe).
Plain-English summary
Invacare Corporation is recalling Bariatric Beds, model BARPKG-IVC 1633, due to a quality issue with the junction box. The defect may cause the junction to omit sparks, which could result in a fire.
The affected 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 were involved in the distribution.
Consumers who have this product should contact Invacare Corporation for further instructions on how to proceed with the recall.
The recalled product
- Product
- Bariatric Bed - BARPKG-IVC 1633
- Manufacturer
- Invacare Corporation
- Category
- Medical Device — Bariatric Bed
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- BARPKG-IVC 1633
Distribution
Part of a larger recall action
This product is one of 4 recalled by Invacare Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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Similar recalls
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