RecallRadar

FDA Drug recall D-0178-2019

Reck Injection, Pharm D Solutions, Houston, Texas --- NDC 69699-1459-50

On 2018-11-07 the FDA classified a Class II recall of Reck Injection, Pharm D Solutions, Houston, Texas --- NDC 69699-1459-50 by Pharm D Solutions, citing lack of Assurance of Sterility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0178-2019
ClassificationClass II
Statusterminated
Initiated2018-09-10
Published2018-11-07
Last updated2026-09-13 11:52 UTC
CompanyPharm D Solutions
DistributionUS

Product

Reck Injection, Pharm D Solutions, Houston, Texas --- NDC 69699-1459-50

Reason

Lack of Assurance of Sterility

Identifiers

code_info
Lot: 03262018:11 Discard by: 4/25/2018; 04102018:38 Discard by: 5/10/2018; 05312018:63 Discard by: 6/30/2018; 05032018:…Lot: 03262018:11 Discard by: 4/25/2018; 04102018:38 Discard by: 5/10/2018; 05312018:63 Discard by: 6/30/2018; 05032018:97 Discard by: 6/2/2018; 06082018:24 Discard by: 7/8/2018; 05212018:80 Discard by: 6/20/2018; 07102018:60 Discard by: 8/9/2018; 06202018:44 Discard by: 7/19/2018; 07232018:08 Discard by: 8/22/2018; 07022018:62 Discard by: 8/1/2018; 08292018:95 Discard by: 9/28/2018; 08202018:61 Discard by: 9/19/2018

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0178-2019%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.