RecallRadar

FDA Drug recall D-0871-2017

morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100…

On 2017-06-07 the FDA classified a Class II recall of morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100… by Sca Pharmaceuticals, citing lack of assurance of sterility: Product bags leaking at seam.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0871-2017
ClassificationClass II
Statusterminated
Initiated2017-05-18
Published2017-06-07
Last updated2026-09-13 11:51 UTC
CompanySca Pharmaceuticals
DistributionUS

Product

morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100 mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-55

Reason

Lack of assurance of sterility: Product bags leaking at seam.

Identifiers

code_infoLOT # 20170508@48, Use By: 08/06/17; 20170505@19, Use By: 08/03/17

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-0871-2017%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.