Recall Register

Cochlear Americas Inc.: FDA recalls

FDA enforcement reports name Cochlear Americas Inc. as the recalling firm in 3 events. The events have 3 product records. The recalls started from 2014 to 2018. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

3 events, newest first.

FDA enforcement events of Cochlear Americas Inc.
InitiatedProduct (first record)TypeClassRecordsStatus
18 Dec 2018Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)DeviceClass II1Terminated
5 Jun 2015Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear” Nucleus Sterile Silicone Template is used in the sterile field to check the size of the periosteal pocket, the shape and depth of the implant well and appropriate positions for tie down holesDeviceClass II1Terminated
9 Apr 2014Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to ensure the soft tissue thickness is equal to or less than 6 mm. For use with Baha Attract hearing system.DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

Cochlear Americas Inc.: events for each product type
TypeEvents
Device3
Cochlear Americas Inc.: events in each class
ClassEvents
Class II3
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
0

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of Cochlear Americas Inc., by the year that the recall started. The largest year is 2014, with 1 event.

Official channels

Cite this page

Recall Register. Cochlear Americas Inc.: FDA recalls. https://recallregister.com/firm/cochlear-americas-inc/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
CO

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of Cochlear Americas Inc. have?
Class II: 3 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of Cochlear Americas Inc.?
FDA event 83970, which the firm started on 18 Dec 2018. The first product in the record is: Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)
How many FDA recalls of Cochlear Americas Inc. have the status Ongoing?
No event has the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.