Linet Spol. S.r.o.: Medical Device Recall in 2019 - (Recall #: Z-0991-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

AVE 2 Birthing Bed

Product Classification:

Class II

Date Initiated: January 7, 2019

Date Posted: March 20, 2019

Recall Number: Z-0991-2019

Event ID: 81927

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.

Status: Terminated

Product Quantity: 253 devices

Code Information:

Serial Numbers 4PPB0091 through 4PPB626

Distribution Pattern:

AL, OK, NJ, OR, WA, CA, MN, LA, AZ, IL, MO, CO, OH, KY, FL, KS, UT, TN, LA, DE, CT, TX

Voluntary or Mandated:

Voluntary: Firm initiated