Hydromorphone Hydrochloride: 8 recalls on record

Recalled by 1 agency: FDA (8).

First recall on record: August 15, 2012. Most recent: March 21, 2018.

Risk classification: Class I: 3 · Class II: 5

Most recent recalls

DateAgencyProduct
March 21, 2018FDAHydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Via…D-0597-2018
September 27, 2017FDAHYDROmorphone HCl Injection, USP, 2 mg/mL, 1mL Single-use vial, packaged in cartons of 25…D-1167-2017
August 16, 2017FDAHydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vi…D-1080-2017
August 16, 2017FDAHydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vi…D-1081-2017
August 16, 2017FDAHydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.…D-1082-2017
October 29, 2014FDAHydromorphone Hydrochloride Injection, USP, 10 mg/mL, Rx only, packaged in a) 1 mL Single…D-0044-2015
October 31, 2012FDAHYDROmorphone HCl Injection, USP, 2 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cart…D-020-2013
August 15, 2012FDAHYDROmorphone HCl Injection, USP, 1 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cart…D-1444-2012

Questions about this brand

How many recalls does Hydromorphone Hydrochloride have?
Recalert has 8 U.S. recalls on record for Hydromorphone Hydrochloride, published between August 15, 2012 and March 21, 2018.
What was the most recent Hydromorphone Hydrochloride recall?
FDA recall D-0597-2018, published March 21, 2018: Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Hospira, Inc., Lake forest, IL 60045 USA. NDC: 0409-2634-01
Which agencies have recalled Hydromorphone Hydrochloride products?
Hydromorphone Hydrochloride products appear in recalls from: FDA (8).

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