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De Soutter Medical
DE SOUTTER MEDICAL LIMITED · Model 16650 · UDI-DI 05051471125643
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Prescription
10
510(k) clearances
1,030
Adverse events (1 deaths)
54
Recalls
45
Facilities
Description
ZIMMER HOSE - 3 METRE WITH DIN PROBE (06001810863)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-02-14 | Pro-Dex Inc | Incorrect Unique Device Identifier/GTIN code was used on product. |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| 2016-10-06 | The Anspach Effort, Inc. | Supplied Directions for Use (DFU) did not contain a recommended service interval. |
| 2016-03-11 | MicroAire Surgical Instruments, LLC | MicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end users and were missing the lock and unlock symbol markings on them. |
| 2013-12-09 | Aesculap, Inc. | Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of the handpiece. |
| 2008-02-21 | Linvatec Corp. | Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s) of the blister pack |
| 2008-02-21 | Linvatec Corp. | Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s) of the blister pack |
| 2008-02-21 | Linvatec Corp. | Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s) of the blister pack |
| 2008-02-21 | Linvatec Corp. | Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s) of the blister pack |
| 2008-02-21 | Linvatec Corp. | Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s) of the blister pack |
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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.