D-0700-2018 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- May 2, 2018
- Initiation Date
- April 11, 2018
- Termination Date
- September 15, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4192 syringes
Product Description
Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-127-10
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 Pattern
Nationwide in the USA
Code Information
Lots: MOR022318NWDSA, MOR022318NWDSB, MOR022318NWDSC, MOR022318NWDSD, MOR022318NWDSE BUD: 05/24/2018