Recalls / Class II
Class IID-0878-2017
Product
MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable, 4g, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0737-32
- Affected lot / code info
- LOT # 20170509@29, Use By: 08/07/17
Why it was recalled
Lack of assurance of sterility: Product bags leaking at seam.
Recalling firm
- Firm
- SCA Pharmaceuticals
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 8821 Knoedl Ct, Little Rock, Arkansas 72205-4600
Distribution
- Quantity
- 40 bags
- Distribution pattern
- Nationwide in the USA
Timeline
- Recall initiated
- 2017-05-18
- FDA classified
- 2017-05-31
- Posted by FDA
- 2017-06-07
- Terminated
- 2018-03-29
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0878-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.