FDA Device Intelligence
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Table, Obstetric (And Accessories)

FDA product code KNC · Class 2 · Obstetrics/Gynecology

55
Registered devices
602
Adverse events
12
Recalls
26
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-05-06Baxter Healthcare CorporationThere is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of th
2021-05-28Hill-Rom, Inc.Latch mechanism on the Lift-Off foot section of the Affinity Four Birthing Bed is damaged, it could potentially cause the installed foot section to be improperl
2016-07-15Hill-Rom, Inc.
2014-06-26Hill-Rom, Inc.The attachment latch mechanism can become bent depending on user handling. Latch mechanism bending could lead to improper engagement of the foot section and th
2012-04-02Hill-Rom, Inc.During review of our last braking system via that field corrective action, the system still did not meet our expectations, which is to eliminate the hazards of
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the
2007-11-21Hill-Rom, Inc.Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the
2006-08-18Hill-Rom, Inc.The cable on the auxiliary outlet may become pinched, which may result in an electrical short with melting of the plastic transformer and the emission of smoke.

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