Stryker Manufacturing S. De R.L. de C.V.
⚠️ Moderate Risk
FEI: 3004555998 • La Masa Tijuana • MEXICO
FEI Number
3004555998
Location
La Masa Tijuana
Country
MEXICOAddress
Ave Las Brisas No. 1200, , La Masa Tijuana, , Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/14/2022 | 80FYAGOWN, SURGICAL | Division of Southeast Imports (DSEI) | |
| 12/14/2022 | 80FYAGOWN, SURGICAL | Division of Southeast Imports (DSEI) | |
| 12/14/2022 | 80FYAGOWN, SURGICAL | Division of Southeast Imports (DSEI) | |
| 12/14/2022 | 80FYAGOWN, SURGICAL | Division of Southeast Imports (DSEI) | |
| 11/23/2022 | 80FYAGOWN, SURGICAL | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 11/3/2022 | 80FYAGOWN, SURGICAL | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Stryker Manufacturing S. De R.L. de C.V.'s FDA import refusal history?
Stryker Manufacturing S. De R.L. de C.V. (FEI: 3004555998) has 6 FDA import refusal record(s) in our database, spanning from 11/3/2022 to 12/14/2022.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Stryker Manufacturing S. De R.L. de C.V.'s FEI number is 3004555998.
What types of violations has Stryker Manufacturing S. De R.L. de C.V. received?
Stryker Manufacturing S. De R.L. de C.V. has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Stryker Manufacturing S. De R.L. de C.V. come from?
All FDA import refusal data for Stryker Manufacturing S. De R.L. de C.V. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.