Home › MEDTRONIC SOFAMOR DANEK, INC. › Medtronic Reusable Instruments
Medtronic Reusable Instruments
MEDTRONIC SOFAMOR DANEK, INC. · Model CDS3A · UDI-DI 00643169100725
10
510(k) clearances
456
Adverse events (5 deaths)
5
Recalls
99
Facilities
Description
CEMENT GUN AND BONE FILLER CDS3A SIZE 3
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-02-28 | Zimmer Biomet, Inc. | Lack of an adequate sterilization validation |
| 2015-08-20 | Orthovita, Inc., dBA Stryker Orthobiologics. | Two isolated instances of holes in the outer header bag component of the double barrier sterile packaging configuration |
| 2015-05-14 | BIOMET FRANCE S.A.R.L. | The pin which maintains the knob button, may disconnect and become lost. This may result in a delay of surgery to obtain a new Optigun and detect/retrieve the pin, and may necessi |
| 2012-01-13 | Stryker Instruments Div. of Stryker Corporation | The firm identified two complaints have been reported indicating that the product inside the package did not match with the label information. The product was labeled as Flat Proxi |
| 2011-03-31 | Orthovita, Inc. | Recalling firm has discovered through internal testing that the Cortoss(TM) Delivery Gun may abrade its packaging material under certain transportation and handling conditions. Th |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.