FDA Drug Recalls

Recalls / Class II

Class IID-0702-2018

Product

NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Syringe. Premier Pharmacy Labs. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-234-14.

Affected lot / code info
Lot: NEO022218SVDS BUD: 8/21/2018

Why it was recalled

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.

Recalling firm

Firm
Premier Pharmacy Labs Inc
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
8265 Commercial Way, N/A, Weeki Wachee, Florida 34613-4511

Distribution

Quantity
600 syringes
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2018-04-11
FDA classified
2018-04-26
Posted by FDA
2018-05-02
Terminated
2020-09-15
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0702-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls