Home / Recalls / Merete Medical GmbH / Z-0438-2021

Z-0438-2021 Class II Terminated

Recalled by Merete Medical GmbH — Berlin

Recall Details

Product Type
Devices
Report Date
November 18, 2020
Initiation Date
September 18, 2020
Termination Date
May 13, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
144 units

Product Description

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

Reason for Recall

Product may be mislabeled.

Distribution Pattern

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

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

Other recalls by Merete Medical GmbH

  • Z-0650-2022 Class II — Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only (January 18, 2022)
  • Z-0437-2021 Class II — OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia) (September 18, 2020)
  • Z-0435-2021 Class II — OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails (September 18, 2020)
  • Z-0436-2021 Class II — OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur) (September 18, 2020)