PlainRecalls
FDA Drug Moderate Class II Terminated

Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72

Reported: February 27, 2019 Initiated: February 6, 2019 #D-0496-2019

Product Description

Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72

Reason for Recall

Labeling: Incorrect expiration date.

Details

Recalling Firm
Advanced Pharma Inc.
Units Affected
100 syringes
Distribution
PA
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
Fentanyl in 0.9% Sodium Chloride QS 0.5 mL, 5 mcg/0.5 mL with up to 0.1 mL of overfill Injectable Solution, Sterile single use syringe, Rx only, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC 42852-210-72. Recalled by Advanced Pharma Inc.. Units affected: 100 syringes.
Why was this product recalled?
Labeling: Incorrect expiration date.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 27, 2019. Severity: Moderate. Recall number: D-0496-2019.