FDA Device Intelligence
HomeAesculap AG › AESCULAP

AESCULAP

Aesculap AG · Model GC771R · UDI-DI 04046963902933

HAB Prescription
2
510(k) clearances
9,928
Adverse events (3 deaths)
16
Recalls
55
Facilities

Description

RECIP.SAW BLADE 75/12/1.0/1.2MM STERILE

Recalls

DateFirmReason
2018-08-27Arthrex, Inc.The Li-ion Battery Housing for the AR-400 DrillSaw Sports 400 System may not provide a complete seal around the battery, allowing for potential fluid ingress.
2017-02-02Smith & Nephew, Inc.The single use devices are provided sterile and do not have an expiration date on the label.
2017-02-02Smith & Nephew, Inc.The single use devices are provided sterile and do not have an expiration date on the label.
2017-02-02Smith & Nephew, Inc.The single use devices are provided sterile and do not have an expiration date on the label.
2017-02-02Smith & Nephew, Inc.The single use devices are provided sterile and do not have an expiration date on the label.
2017-02-02Smith & Nephew, Inc.The single use devices are provided sterile and do not have an expiration date on the label.
2017-02-02Smith & Nephew, Inc.The single use devices are provided sterile and do not have an expiration date on the label.
2016-09-28Zimmer Biomet, Inc.Complaints have been reported that the handpiece is inoperable. The investigation found that the complaints were related to the lack of preventative maintenance contrary to what is
2015-11-10Zimmer, Inc.The firm identified a malfunction which made it possible for a handpiece to start by itself when the power source is connected.
2015-11-10Zimmer, Inc.The firm identified a malfunction which made it possible for a handpiece to start by itself when the power source is connected.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.