Recalls / Class III
Class IIID-0473-2018
Product
Calcium Acetate Capsules, 667 mg, 200 Capsules per bottle, Rx Only. Manufactured by Nostrum Laboratories, Inc. Kansas City, MO 64120. NDC 29033-026-02
- Affected lot / code info
- Lot: CAL173502; Exp. 09/19
Why it was recalled
Presence of Foreign Tablets/Capsules
Recalling firm
- Firm
- Nostrum Laboratories Inc
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 1800 N Topping Ave, N/A, Kansas City, Missouri 64120-1228
Distribution
- Quantity
- 1,439,000 oral capsules
- Distribution pattern
- Nationwide
Timeline
- Recall initiated
- 2018-02-13
- FDA classified
- 2018-02-20
- Posted by FDA
- 2018-02-28
- Terminated
- 2018-12-13
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0473-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.