PlainRecalls
FDA Drug Moderate Class II Terminated

HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10

Reported: May 8, 2019 Initiated: April 26, 2019 #D-1251-2019

Product Description

HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10

Reason for Recall

Sub-potency

Details

Recalling Firm
Advanced Pharma Inc.
Units Affected
560 bags
Distribution
Nationwide in the US
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10. Recalled by Advanced Pharma Inc.. Units affected: 560 bags.
Why was this product recalled?
Sub-potency
Which agency issued this recall?
This recall was issued by the FDA Drug on May 8, 2019. Severity: Moderate. Recall number: D-1251-2019.