Recalls / Class II
Class IID-0851-2018
Product
SDA Senna Syrup (Sennosides 8.8mg), packaged in 8 FL. OZ. (236 mL) bottles, Distributed by SDA Laboratories 280 Railroad Avenue, Greenwich CT 06830, NDC 66424-562-08, UPC 366424562082
- Brand name
- Senna Syrup
- Generic name
- Sennosides A And B
- Active ingredient
- Sennosides A And B
- Route
- Oral
- NDC
- 66424-562
- FDA application
- M007
- Affected lot / code info
- Lot #: 47070042, Exp. 09/18
Why it was recalled
CGMP Deviations: Products are being recalled due to an out of specification total aerobic microbial count in a water sample.
Recalling firm
- Firm
- RIJ Pharmaceutical LLC
- Manufacturer
- SDA Laboratories, Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 40 Commercial Ave, N/A, Middletown, New York 10941-1444
Distribution
- Quantity
- 3537 bottles
- Distribution pattern
- Nationwide in the USA
Timeline
- Recall initiated
- 2018-05-07
- FDA classified
- 2018-06-08
- Posted by FDA
- 2018-06-20
- Terminated
- 2023-04-07
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-0851-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.