Reported Dec 17, 2014 · Terminated
Hudson cranial drill sets (w/ brace and 5 attachments) are bone cutting and drilling instruments that are used without…
Instrumed International, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Instrumed International, Inc. · 626 Cooper Ct · Schaumburg, IL · 60173-4537
Is this the product you have?
- Hudson cranial drill sets (w/ brace and 5 attachments) are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the Symmetry Surgical, Medfix International, Stealth Surgical, and Boss Instruments brand names.
- Lot codes and dates
21 of 21 products
Products covered by this recall Model / number Product as published — Hudson Cranial Drill Set (w/ brace and 5 attachments) 600-00616Instrumed — Trade Name: Symmetry Surgical — Symmetry Surgical Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) 57-6000Symmetry Surgical — Lot Number: 110212. 2) Instrumed Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) 600-00616Instrumed — Trade Name: Medfix International — Medfix International Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) MF223-1672Medfix International — Lot Number: 110212. 3) Instrumed Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) 600-00616Instrumed — Trade Name: Stealth Surgical — Stealth Surgical Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) SS2135Stealth Surgical — Lot Number: 110212. 4) Instrumed Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) 600-00616Instrumed — Trade Name: Boss Instruments — Boss Instruments Product Name: Hudson Cranial Drill Set (w/ brace and 5 attachments) 74-0120Boss Instruments - Amount recalled
- 5 Hudson cranial drill sets
This recall covers 28 products
The agency filed one notice per product. You are reading one of them; the other 27 are below.
15 more are in the archive.
Where it was sold
Why it was recalled
The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as "Pre-Amendment" devices.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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