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Bausch & Lomb Incorporated · Model E5754 D · UDI-DI 00757770417629
HKY
Prescription
10
510(k) clearances
11
Adverse events
2
Recalls
64
Facilities
Description
X-WGT F/E5754&E5755 5.5 GR
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a |
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