PlainRecalls
FDA Devices Moderate Class II Terminated

AVE 2 Birthing Bed

Reported: March 20, 2019 Initiated: January 7, 2019 #Z-0991-2019

Product Description

AVE 2 Birthing Bed

Reason for Recall

LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable may fail causing a possible spark or possible exposure to a live conductor.

Details

Recalling Firm
Linet Spol. S.r.o.
Units Affected
253 devices
Distribution
AL, OK, NJ, OR, WA, CA, MN, LA, AZ, IL, MO, CO, OH, KY, FL, KS, UT, TN, LA, DE, CT, TX
Location
Slany, N/A

Frequently Asked Questions

What product was recalled?
AVE 2 Birthing Bed. Recalled by Linet Spol. S.r.o.. Units affected: 253 devices.
Why was this product recalled?
LINET has recently become aware of a potential safety issue for the AVE 2 Birthing Bed caused by the power cable breaking at the bed connection or the orange insulation of the power cable may fail causing a possible spark or possible exposure to a live conductor.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 20, 2019. Severity: Moderate. Recall number: Z-0991-2019.