Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Reported: February 12, 2020 Initiated: December 23, 2019 #Z-0924-2020
Product Description
Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.
Reason for Recall
The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
Details
- Recalling Firm
- Jjgc Industria E Comercio De Materials Dentarios Sa
- Units Affected
- 2
- Distribution
- Distributed to consignees in CA and PA.
- Location
- Curitiba, N/A
Frequently Asked Questions
What product was recalled? ▼
Neodent Tapered Guided Surgery Drill, Article No. 103.436. UDI 07899878030041. The device is a dental burr.. Recalled by Jjgc Industria E Comercio De Materials Dentarios Sa. Units affected: 2.
Why was this product recalled? ▼
The laser engraving of the product incorrectly identifies the 4.3 Tapered Guided Surgery Drill as the "4.3+ Tapered Guided Surgery Drill".
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 12, 2020. Severity: Moderate. Recall number: Z-0924-2020.
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