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Stryker Macroom

⚠️ Moderate Risk

FEI: 3008337808 • Macroom, County Cork Munster • IRELAND

FEI

FEI Number

3008337808

📍

Location

Macroom, County Cork Munster

🇮🇪

Country

IRELAND
🏢

Address

Hartnetts Cross, , Macroom, County Cork Munster, Ireland

Moderate Risk

FDA Import Risk Assessment

35.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

10
Total Refusals
4
Unique Violations
6/16/2020
Latest Refusal
2/8/2018
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
42.5×10%
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

1189×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

3416×

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).

5086×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

32804×

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

DateProductViolationsDivision
6/16/2020
87KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
6/16/2020
87KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
6/16/2020
87KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
6/16/2020
87KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
6/16/2020
87KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
6/16/2020
87KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
7/3/2018
87HWCSCREW, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/3/2018
87HWCSCREW, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/3/2018
87HWCSCREW, FIXATION, BONE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
2/8/2018
87HRSPLATE, FIXATION, BONE
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Stryker Macroom's FDA import refusal history?

Stryker Macroom (FEI: 3008337808) has 10 FDA import refusal record(s) in our database, spanning from 2/8/2018 to 6/16/2020.

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 Macroom's FEI number is 3008337808.

What types of violations has Stryker Macroom received?

Stryker Macroom has been cited for 4 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 Macroom come from?

All FDA import refusal data for Stryker Macroom 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.