Facility

Etac A/S

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3004137175
Establishment type	Manufacture Medical Device
Location	Parallelvej 3 Gedved Midtjylland, DK DK- 8751
Registration status	Active · expires 2026
Parent company	Etac A/S (owner-operator 9058632)
Brand names	Molift UnoSling; Etac Turner Pro; Molift RgoSling; Molift EvoSling; Molift Raiser Pro; Etac Nova; Molift Transfer Pro

Activity by year

Recalls (1)

Devices registered here (1)

Aid, Transfer
Product code IKX (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.5050

Recalls & enforcement

Class IIOngoing2025-11-17
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the …

All facilities operated by Etac A/S

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Etac A/S (FEI 3004137175) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004137175-etac-a-s/

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