FDAFDA · Food and drugs·Recall number D-0867-2020
Ketorolac Trom, 30 mg/1mL Inj. for I.V./I.M. Use, Rx Only, QTY: 1 ml, Repackaged by: RemedyRepack Inc., Indiana, PA 15701 NDC 70518-1239-00
Published February 19, 2020 · Recall initiated: December 27, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- RemedyRepack Inc.
- Distributor
- Product distributed in OK and LA.
- Lot
- Lot # B0444562-060118, exp. 04/2020, B0537002-112118, exp 07/2020
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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