Hager & Meisinger Gmbh: Medical Device Recall in 2020 - (Recall #: Z-2937-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for use in the fabrication of dental devices.

Product Classification:

Class II

Date Initiated: July 15, 2020

Date Posted: September 16, 2020

Recall Number: Z-2937-2020

Event ID: 86147

Reason for Recall:

US-dates between the product package label and the bar code display.

Status: Terminated

Product Quantity: 144 units

Code Information:

LOT R50753

Distribution Pattern:

US Nationwide distribution including in the states of AZ, CA, FL, IN, NY, PA and TX.

Voluntary or Mandated:

Voluntary: Firm initiated