Medical Specialties Distributors, LLC
Country not established
- Devices
- 296
- FDA recalls
- 1
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
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- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
- Withdrawn Registry: GUDID ClassClass:II
- Withdrawn Registry: GUDID ClassClass:I
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Company details
- DUNS number
- 153608369
- [email protected]
- Phone
- 800-967-6400
FDA recalls1
Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.
2012
- 3 Aug 2012 Z-2179-2012 Class II Terminated Devices leaking at the Y-site Distribution: Nationwide Distribution Submission number: K090012