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Table, Obstetrical, Ac-Powered (And Accessories)

FDA product code HDD · Class 2 · Obstetrics/Gynecology

35
Registered devices
4,666
Adverse events
8
Recalls
7
510(k) clearances

Devices with this code

Vibwife — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.NA — STRYKER CORPORATIONAve 2 — L I N E T spol. s r.o.Vibwife — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.NA — STRYKER CORPORATIONAve 2 — L I N E T spol. s r.o.NA — STRYKER CORPORATIONAve 2 — L I N E T spol. s r.o.NA — STRYKER CORPORATIONNA — STRYKER CORPORATIONAve 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.NA — STRYKER CORPORATIONNA — STRYKER CORPORATIONAve 2 — L I N E T spol. s r.o.AVE 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.Ave 2 — L I N E T spol. s r.o.

Recent recalls

DateFirmReason
2020-03-06Linet AmericasThe UDI on the device label indicates incorrect manufacturer.
2019-01-07Linet Spol. S.r.o.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 in
2009-11-16Hill-Rom, Inc.The brakes may not hold or lock.
2007-09-06Hill-Rom, Inc.Brake failure: The brakes may not hold or lock properly.
2005-03-31Stryker MedicalTrendelenburg and reverse trendelenburg features may not function.
2004-01-26Stryker MedicalA potential shock hazard exists if the night light is damaged.
2004-01-26Stryker MedicalA potential shock hazard exists if the night light is damaged.
2004-01-26Stryker MedicalA potential shock hazard exists if the night light is damaged.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.