Skip to main content

Ketorolac Tromethamine Injection, USP, 30 mg per mL, packaged in 1 mL Single Dose Vials (NDC 63323-162-00); 25 x 1 mL Single Dose Vials per tray (NDC 63323-162-01); For IM or IV use, Rx only, Fresenius Kabi, Lake Zurich, IL 60047.

Drug Recall

Official source record

Recall number
D-0245-2021
Event ID
87082
Classification
Class I
Status
Terminated
Recalling company
Fresenius Kabi USA, LLC
Reason for recall
Presence of Particulate Matter - found in reserve sample vials at the firm.
Report date
February 3, 2021
Recall initiation date
December 23, 2020
Termination date
June 9, 2023
Distribution pattern
Nationwide USA and Puerto Rico

Drug product identifiers

Manufacturer
Fresenius Kabi USA, LLC
Brand name
KETOROLAC TROMETHAMINE
Generic name
KETOROLAC TROMETHAMINE
Substance name
KETOROLAC TROMETHAMINE
Product NDCs
63323-161; 63323-162
Package NDCs
63323-161-00; 63323-161-01; 63323-162-00; 63323-162-01; 63323-162-02; 63323-162-03; 63323-162-11; 63323-162-51
Routes
INTRAMUSCULAR; INTRAVENOUS

Where this information comes from

View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this medication?

Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.

Where can I find more official information?

The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.