FDA Drug Recalls

Recalls / Class II

Class IID-0270-2015

Product

2Ml HCG 10,000 U/ MB12 - 12,000 MCG/10 Ml Inj, 0.25ML (250IU), Rx, Perry Drug Compounding Pharmacy, Overland Park, KS ---NDC 88888-7945-17

Affected lot / code info
141016A, 11/16/14

Why it was recalled

Lack of sterility assurance;All lots of sterile products compounded by the pharmacy that are within expiry were recalled due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Recalling firm

Firm
Perry Drug Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
12200 W 106th St Ste 140, N/A, Overland Park, Kansas 66215-2305

Distribution

Quantity
1 vial
Distribution pattern
Kansas and Missouri

Timeline

Recall initiated
2014-11-07
FDA classified
2014-11-24
Posted by FDA
2014-12-03
Terminated
2015-11-03
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0270-2015. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.