Recall Register

Drug recall: 0.9% SODIUM CHLORIDE Irrigation, USP 1000 mL Semi-Rigid Bottle, Rx only, Manufactured for ICU Medical, Inc., Lake…

Class II FDA enforcement event 87484. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Presence of particulate matter.one confirmed customer report of particulate matter within two semi-rigid bottles identified prior to use

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

ICU Medical Inc started this drug recall on 9 Mar 2021. The firm address in the FDA record is in Lake Forest, IL. FDA put the recall in Class II. FDA event 87484 has 1 product record. The first FDA enforcement report date is 31 Mar 2021. The record gives the status Terminated, with the termination date 28 Sep 2022.

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.

Distributed Nationwide in the USA to include Puerto Rico

Recalling firm

ICU Medical Inc, Lake Forest, IL.

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

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

Products

1 product record in the event.

FDA event 87484: product records
Recall numberProductQuantityClassStatusReport date
D-0313-20210.9% SODIUM CHLORIDE Irrigation, USP 1000 mL Semi-Rigid Bottle, Rx only, Manufactured for ICU Medical, Inc., Lake Forest, Illinois, 60045 USA. NDC 0990-7138-09425,628 bottlesClass IITerminated31 Mar 2021

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

Drug events that started in 2021
299
Share of these events in Class II
60%
Product records in this event
1Median of the firm: 2
Events of the firm on the register
75

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 87484. https://recallregister.com/fda/ii/87484/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA drug 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: Distributed Nationwide in the USA to include Puerto Rico
What quantity of product is in FDA event 87484?
The FDA record gives this quantity: 425,628 bottles
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many drug recalls of 2021 have the same class?
60% of the 299 drug events that started in 2021 are in Class II.