OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
Reported: November 18, 2020 Initiated: September 18, 2020 #Z-0437-2021
Product Description
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
Reason for Recall
Product may be mislabeled.
Details
- Recalling Firm
- Merete Medical GmbH
- Units Affected
- 215 units
- Distribution
- Product was distributed in US - CA, IL, MD, OH, and NJ
- Location
- Berlin
Frequently Asked Questions
What product was recalled? ▼
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia). Recalled by Merete Medical GmbH. Units affected: 215 units.
Why was this product recalled? ▼
Product may be mislabeled.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 18, 2020. Severity: Moderate. Recall number: Z-0437-2021.
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