RecallRadar

FDA Drug recall D-0699-2018

Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613

On 2018-05-02 the FDA classified a Class II recall of Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613 by Premier Pharmacy Labs, citing lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0699-2018
ClassificationClass II
Statusterminated
Initiated2018-04-11
Published2018-05-02
Last updated2026-09-13 11:52 UTC
CompanyPremier Pharmacy Labs
DistributionUS

Product

Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-129-10

Reason

Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

Identifiers

code_infoLots: MOR030518IJDSA, MOR030518IJDSB, MOR030518IJDSC, MOR030518IJDSD, MOR030518IJDSE BUD: 06/03/2018;

Status history

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

Other recalls by Premier Pharmacy Labs

All Premier Pharmacy Labs recalls

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0699-2018%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.