Home/Recalls/FDA-D-0506-2026
FDA DrugsClass II

fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 ...

Published: May 6, 2026Recall ID: D-0506-2026Category: drugsCountry: US

Reason for Recall / Hazard

cGMP deviations.

Product Description & Identification

fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.

Affected Products

fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.

Additional Source Details

FieldValue
CityHouston
StateTX
Event id98694
Address 19265 Kirby Dr
Code infoLot 022326203650432; Exp Date 06/25/2026
Postal code77054-2520
Report date20260506
Product typeDrugs
Product quantity150 syringes
Reason for recallcGMP deviations.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260401
Initial firm notificationLetter
Center classification date20260428

Overview

  • Recalling FirmWells Pharma of Houston LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionU.S. Nationwide.
Official Agency Alert