FDA recall D-0701-2018

Product

Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Sterile Single-Dose Syringe. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-249-10

Reason for recall

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.

Distribution

Nationwide in the USA

Key facts

Status

Terminated

Initiation date

2018-04-11

Report date

2018-05-02

Termination date

2020-09-15

Voluntary/Mandated

Voluntary: Firm initiated

Location

Weeki Wachee, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0701-2018