CLASS II Drug recall · Reported 27 Mar 2019 · FDA Enforcement Report

Glycopyrrolate Injectable Solution 1 mg/ (0.2 mg per mL) recalled

Advanced Pharma is recalling Glycopyrrolate Injectable Solution 1 mg/ (0.2 mg per mL), Sterile single use syringe, distributed nationwide in the US. The recall was initiated on 13 Mar 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 12/05/18 0710 82867S Exp. 5/4/2019; 10/24/18 0014 82867S Exp. 3/23/2019; 11/01/18 8800 82867S Exp. 3/31/2019
Quantity recalled2580 syringes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1021-2019
FDA event ID
82398
Recalling firm
Advanced Pharma, Houston, TX
Classification
Class II
Status
Terminated
Recall initiated
13 Mar 2019
FDA classified
21 Mar 2019
Reported
27 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

13 Mar 2019Recall initiated by company
21 Mar 2019Classified by FDA+8 days
27 Mar 2019Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack of Assurance of Sterility

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Glycopyrrolate Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-828-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility

Which lots are affected?

Lot: 12/05/18 0710 82867S Exp. 5/4/2019; 10/24/18 0014 82867S Exp. 3/23/2019; 11/01/18 8800 82867S Exp. 3/31/2019

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

18 other products · FDA event 82398

This product is part of a recall event; the main page for the event is Morphine Sulfate 30 mg/ (1 mg/mL) Injectable Solution recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIMorphine Sulfate 30 mg/ (1 mg/mL) Injectable Solution recalledAdvanced PharmaSterilityNationwide
CLASS IIfentaNYL 1000 mcg/ Injectable Solution Fentanyl 0.9% Sodium recalledAdvanced PharmaSterilityNationwide
CLASS IIPhenylephrine HCl, 1 mg in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS II2% Lidocaine HCl Injectable Solution, 60 mg recalled by Advanced PharmaAdvanced PharmaSterilityNationwide
CLASS IIHeparin per mL) Injectable Solution in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS IIPhenylephrine HCl, 400 mcg in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS IIEsmolol HCl Injectable Solution 100 mg recalled by Advanced PharmaAdvanced PharmaSterilityNationwide
CLASS IIfentaNYL 2500 mcg/ Injectable Solution recalled by Advanced PharmaAdvanced PharmaSterilityNationwide
CLASS IIPhenylephrine HCl, 1 mg in Sterile Water for Injection recalledAdvanced PharmaSterilityNationwide
CLASS IIGlycopyrrolate 0.6 mg/ (0.2 mg per mL) Injectable Solution recalledAdvanced PharmaSterilityNationwide
CLASS II2% Lidocaine HCl Injectable Solution, 100 mg recalled by Advanced PharmaAdvanced PharmaSterilityNationwide
CLASS IIPhenylephrine HCl, 800 mcg in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS IIMidazolam Benzodiazepine 50 mg recalled by Advanced PharmaAdvanced PharmaSterilityNationwide
CLASS IIPhenylephrine HCl, 500 mcg in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS IIHeparin in 0.45% Sodium Chloride, QS, Injectable Solution recalledAdvanced PharmaSterilityNationwide
CLASS IIHYDROmorphone HCl 1 mg in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS IIPhenylephrine HCl, 1,200 mcg in 0.9% Sodium Chloride recalledAdvanced PharmaSterilityNationwide
CLASS IINeostigmine Methylsulfate Injection Solution 5 mg recalledAdvanced PharmaSterilityNationwide

More recalls from Advanced Pharma

All 99

Other Glycopyrrolate recalls

All 43