Merete Medical GmbH: Medical Device Recall in 2020 - (Recall #: Z-0438-2021)

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:

OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus)

Product Classification:

Class II

Date Initiated: September 18, 2020

Date Posted: November 18, 2020

Recall Number: Z-0438-2021

Event ID: 86526

Reason for Recall:

Product may be mislabeled.

Status: Terminated

Product Quantity: 144 units

Code Information:

Lot Number Use By Date MS1912994R 6/4/2025 MS1811555R 7/24/2025 MS1913023R 6/4/2025 MS1811556R 7/24/2025 MS1913024R 6/4/2025 MS1913024R 6/4/2025 MS1811557R 7/24/2025 MS1913027R 6/4/2025 MS1811585R 7/23/2025 MS1913028R 6/4/2025 MS1811604R 7/23/2025 MS1913029R 6/4/2025 MS1913029R 6/4/2025 MS1811605R 7/23/2025 MS1913038R 6/4/2025 MS1811606R 7/23/2025 MS1811607R 6/4/2025 MS1811607R1 7/23/2025 MS1913039R 6/4/2025 MS1811624R 7/23/2025 MS1811673R 6/4/2025 MS1811625R 7/23/2025 MS1811673R1 7/23/2025 MS1811634R 6/4/2025 MS1811634R1 7/23/2025 MS1913041R 6/4/2025 MS1811623R 7/24/2025 MS1913042R 6/4/2025 MS1811635R 7/24/2025 MS1913043R 6/4/2025 MS1913043R 6/4/2025 MS1811636R 7/24/2025

Distribution Pattern:

Product was distributed in US - CA, IL, MD, OH, and NJ

Voluntary or Mandated:

Voluntary: Firm initiated