BD Announces FDA Classifications for August 4th Recalls of ... | 合法醫療器材資訊網

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These recall notices provide current information on medical device recalls. For questions pertaining to a specific medical device recall, please see the contact ... Read More

2020年3月10日 — BD Provides Update on Feb. 4, 2020 Voluntary Recall of the BD Alaris™ System PC Units and Modules. When a company announces a recall, ... Read More

2020年3月6日 — Becton Dickinson (BD) CareFusion 303 Inc. Recalls Alaris System Infusion Pumps Due to Software and System Errors ... The FDA has identified ... Read More

2020年9月1日 — Three of the situations described in this recall, which BD announced on June 30, 2020, have been designated as Class I recalls by the U.S. ... Read More

List of Medical Device recalls in 2020. ... Becton Dickinson (BD) CareFusion 303 Inc. Recalls Alaris™ Syringe and Alaris™ PCA Modules Due to Potential ... Read More

2020年9月14日 — Becton Dickinson (BD) CareFusion 303 Recalls Alaris System Infusion Pumps Due to Damaged Inter-Unit Interface Connectors, Loose or ... Read More

2021年4月16日 — Please note, this recall is separate from the BD Alaris Pump Module 8100 keypad recall dated August 4, 2020. Who May be Affected. Health care ... Read More

2020年8月3日 — On March 6, 2020, the U.S. Food and Drug Administration announced that it had classified the Becton Dickinson Alaris System infusion pump ... Read More

2021年4月26日 — The announcement coincided with software recalls issued by BD. Multiple hardware recalls for the Alaris system throughout 2020 and 2021 ... Read More