Recall Register

Device recall: 6376 M-1 Cot Fastener, catalog no. 6376000000

Class II FDA enforcement event 79817. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

The Operations Manual and Maintenance Manual are missing various warnings and contain incorrect information.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Stryker Medical Division of Stryker Corporation started this device recall on 9 Mar 2018. The firm address in the FDA record is in Portage, MI. FDA put the recall in Class II. FDA event 79817 has 2 product records. The first FDA enforcement report date is 9 May 2018. The record gives the status Terminated, with the termination date 9 Apr 2019.

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 .

Distribution

In the words of FDA.

Product distributed to the Netherlands

Recalling firm

Stryker Medical Division of Stryker Corporation, Portage, MI.

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

FDA records how the recall started: Voluntary: Firm initiated.

Products

2 product records in the event.

FDA event 79817: product records
Recall numberProductQuantityClassStatusReport date
Z-1598-20186376 M-1 Cot Fastener, catalog no. 637600000059Class IITerminated9 May 2018
Z-1599-20186381 M-1 Cot Fastener, catalog no. 63810000003Class IITerminated9 May 2018

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.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

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

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2018
1,074
Share of these events in Class II
92%
Product records in this event
2Median of the firm: 1
Events of the firm on the register
37

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 79817. https://recallregister.com/fda/ii/79817/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Product distributed to the Netherlands
What quantity of product is in FDA event 79817?
The event has 2 product records. The first record gives this quantity: 59
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2018 have the same class?
92% of the 1,074 device events that started in 2018 are in Class II.