Class IIOngoingZ-0966-2025
Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 9mm - Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Adept Medical Ltd recalls
The FDA has posted 8 enforcement recalls from Adept Medical Ltd since 2025, none of them Class I (most serious). Most recent report: Jan 29, 2025.
Class II: 8
Latest recalls
View all 8 in the recall browser →Class IIOngoingZ-0964-2025
Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 6mm - Double - Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Class IIOngoingZ-0969-2025
Adept Medical Ltd recalls Otological Ventilation Tube - Donaldson - Blue Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Class IIOngoingZ-0965-2025
Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 9mm - Double - Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Class IIOngoingZ-0967-2025
Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 12mm - Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Class IIOngoingZ-0963-2025
Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 6mm - Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Class IIOngoingZ-0968-2025
Adept Medical Ltd recalls Otological Ventilation Tube - T-Tube 12mm - Double - Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Class IIOngoingZ-0970-2025
Adept Medical Ltd recalls Otological Ventilation Tube - Donaldson - Double - Blue Silicone
Lack of 510(k) clearance.
- Tympanostomy Tube
- Device Design
Adept Medical LtdJan 29, 2025
Firm name as filed with the FDA: “Adept Medical Ltd”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.