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Adapter

C. R. Bard, Inc. · Model 9019500 · UDI-DI 10801741051385

GCY Prescription

510(k) clearances

4,734

Adverse events (13 deaths)

107

Recalls

219

Facilities

Description

Small Blue Adapter, for use with ReliaVac 400 and ReliaVac 100 Closed Wound Suction Systems and 1/8" Round Silicone Drains

Recalls

Date	Firm	Reason
2018-11-05	COVIDIEN LLC	The product was released into commercial distribution while subject to importation refusal.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.
2017-04-21	Cardinal Health 200, LLC	Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

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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.