Hilbro (PVT) Ltd.
⚠️ Moderate Risk
FEI: 3374 • Sialkot • PAKISTAN
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
STAINSTEEL
The article appears to be a device whose quality falls below that which it purports or is represented to possess, in that instrument is represented as stainless steel but does not meet requirements for such steel for surgical instruments.
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
DE IMP GMP
The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/6/2012 | 78FHQHOLDER, NEEDLE | 290DE IMP GMP | Chicago District Office (CHI-DO) |
| 7/28/2011 | 74DWPDILATOR, VESSEL, SURGICAL | 290DE IMP GMP | Cincinnati District Office (CIN-DO) |
| 7/28/2011 | 79GDGHOOK, SURGICAL, GENERAL & PLASTIC SURGERY | 290DE IMP GMP | Cincinnati District Office (CIN-DO) |
| 7/28/2011 | 78FHQHOLDER, NEEDLE | 290DE IMP GMP | Cincinnati District Office (CIN-DO) |
| 7/28/2011 | 79HTDFORCEPS | 290DE IMP GMP | Cincinnati District Office (CIN-DO) |
| 7/28/2011 | 79HTDFORCEPS | 290DE IMP GMP | Cincinnati District Office (CIN-DO) |
| 8/20/2010 | 79LRWSCISSORS, GENERAL USE, SURGICAL | 480STAINSTEEL | New York District Office (NYK-DO) |
| 9/9/2009 | 76EMIFILE, BONE, SURGICAL | 480STAINSTEEL | New York District Office (NYK-DO) |
| 6/24/2009 | 79LRWSCISSORS, GENERAL USE, SURGICAL | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 79FZYHAMMER, SURGICAL | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 86HNFSCISSORS, OPHTHALMIC | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 79GADRETRACTOR, SURGICAL, GENERAL & PLASTIC SURGERY | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 79GDRSAW, MANUAL AND ACCESSORIES | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 77KALRETRACTOR, ENT | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 79GENFORCEPS, GENERAL & PLASTIC SURGERY | Chicago District Office (CHI-DO) | |
| 6/24/2009 | 79GENFORCEPS, GENERAL & PLASTIC SURGERY | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Hilbro (PVT) Ltd.'s FDA import refusal history?
Hilbro (PVT) Ltd. (FEI: 3374) has 16 FDA import refusal record(s) in our database, spanning from 6/24/2009 to 1/6/2012.
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. Hilbro (PVT) Ltd.'s FEI number is 3374.
What types of violations has Hilbro (PVT) Ltd. received?
Hilbro (PVT) Ltd. has been cited for 3 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 Hilbro (PVT) Ltd. come from?
All FDA import refusal data for Hilbro (PVT) Ltd. 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.