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Razor, Surgical

FDA product code LWK · Class 1 · General, Plastic Surgery

106
Registered devices
227
Adverse events
6
Recalls
4
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-01-123M Company - Health Care Business3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in m
2024-01-123M Company - Health Care Business3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in m
2019-09-06Medline Industries IncThe recall is being conducted due to a potential defective component on the circuit board causing the charger base to overheat which could result in a charger b
2019-01-143M Company - Health Care Business3M has recently received reports involving the 3MTM Surgical Clipper by Remington, Model 9602, overheating in mobile/field EMS situations while charging from a
2018-02-023M Company - Health Care BusinessFailure to follow proper charging practices can result in lithium-ion battery degradation, characterized by excessive heat during operation or failure to proper
2015-07-08Medline Industries IncCharging base of surgical clippers overheats and smokes.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.