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Ambu

Technomed Engineering B.V. · Model 74725-60/24 · UDI-DI 08720791370893

GXZIKT Prescription
10
510(k) clearances
329
Adverse events
21
Recalls
65
Facilities

Description

Ambu® Subdermal Corkscrew 2.5m wire 4x6 colors 24pcs

Recalls

DateFirmReason
2021-12-08Technomed EuropeThere is a high risk of the blue hub detaching from the corkscrew needle, resulting the the needle remaining in the patient's scalp.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.
2010-02-01Stryker Instruments Div. of Stryker CorporationDefects include, but not limited to: Not sterile, not properly labeled, drugs and swabs may be ineffective, and catheter tips may break in patients.

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Data 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.