Recalls / Class II
Class IID-0978-2017
Product
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 15 mMol (22 mEq K+) Total Approximate Volume 255 mL, Rx only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0841-32
- Affected lot / code info
- Lot #: 20170602@29, Exp 7/17/2017
Why it was recalled
Lack of sterility assurance
Recalling firm
- Firm
- SCA Pharmaceuticals
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 8821 Knoedl Ct, Little Rock, Arkansas 72205-4600
Distribution
- Quantity
- 20 bags
- Distribution pattern
- LA, PA, NY, WI
Timeline
- Recall initiated
- 2017-06-21
- FDA classified
- 2017-07-13
- Posted by FDA
- 2017-07-19
- Terminated
- 2019-04-03
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0978-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.