Reported Feb 19, 2020 · Terminated

Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only, QTY: 1 ml, Repackaged by: RemedyRepack Inc., Indiana, PA…

RemedyRepack Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: RemedyRepack Inc. · 625 Kolter Dr Ste 4 · Indiana, PA · 15701-3571

Is this the product you have?

  • Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only
  • QTY1 ml
  • Repackaged byRemedyRepack Inc., Indiana, PA 15701 NDC 70518-1239-00
Lot codes and dates
    • Lot # B0444562-060118
    • exp. 04/2020
    • B0537002-112118
    • exp 07/2020
Amount recalled
75 1 ml vials

Where it was sold

Why it was recalled

Stop using this product now

Presence of Particulate Matter: Medication relabeled at facility was recalled by the manufacturer due to small black particles noticed during routine visual inspection. of retain samples.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 18, 2020 · Data as of Sep 19, 6:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.