RecallRadar

FDA Drug recall D-0384-2017

QUAD2 (PAP/PHEN/ALPROS/ATRO) 9 mg/1 mg/10 mg/0.1 mg/mL Injectable a) 2 mL and b) 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL

On 2017-01-11 the FDA classified a Class II recall of QUAD2 (PAP/PHEN/ALPROS/ATRO) 9 mg/1 mg/10 mg/0.1 mg/mL Injectable a) 2 mL and b) 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL by Wells Pharmacy Network, citing lack of Assurance of Sterility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0384-2017
ClassificationClass II
Statusterminated
Initiated2016-09-21
Published2017-01-11
Last updated2026-09-13 11:51 UTC
CompanyWells Pharmacy Network
DistributionUS

Product

QUAD2 (PAP/PHEN/ALPROS/ATRO) 9 mg/1 mg/10 mg/0.1 mg/mL Injectable a) 2 mL and b) 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL

Reason

Lack of Assurance of Sterility

Identifiers

code_info
All lot codes of product prepared between 02/22/2016 and 09/14/2016, within expiry. a) Known lot code: 04222016@8,…All lot codes of product prepared between 02/22/2016 and 09/14/2016, within expiry. a) Known lot code: 04222016@8, 06142016@42, 08152016@17 b) Known lot code: 03312016@8, 05182016@15, 08092016@18

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0384-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.