HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Reported: August 3, 2022 Initiated: May 26, 2022 #Z-1468-2022
Product Description
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Reason for Recall
Due to Titanium plasma coating not present implant.
Details
- Recalling Firm
- Paragon 28, Inc.
- Units Affected
- 9 implants
- Distribution
- U.S. Nationwide distribution in the states of AL, CA, GA, IL and KY.
- Location
- Englewood, CO
Frequently Asked Questions
What product was recalled? ▼
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile). Recalled by Paragon 28, Inc.. Units affected: 9 implants.
Why was this product recalled? ▼
Due to Titanium plasma coating not present implant.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 3, 2022. Severity: Moderate. Recall number: Z-1468-2022.
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