Provocholine pre-diluted in 0.9% Sodium Chloride Set II syringes, 0.0625mg/mL,3 mL; 0.25 mg/mL 3mL; 1 mg/mL 3mL; 4 mg/mL 3mL; 16 mg/ml 3mL, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0674-80
Reported: July 20, 2016 Initiated: April 20, 2016 #D-1290-2016
Product Description
Provocholine pre-diluted in 0.9% Sodium Chloride Set II syringes, 0.0625mg/mL,3 mL; 0.25 mg/mL 3mL; 1 mg/mL 3mL; 4 mg/mL 3mL; 16 mg/ml 3mL, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0674-80
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Pharmakon Pharmaceuticals, Inc.
- Units Affected
- 142
- Distribution
- Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
- Location
- Noblesville, IN
Frequently Asked Questions
What product was recalled? ▼
Provocholine pre-diluted in 0.9% Sodium Chloride Set II syringes, 0.0625mg/mL,3 mL; 0.25 mg/mL 3mL; 1 mg/mL 3mL; 4 mg/mL 3mL; 16 mg/ml 3mL, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0674-80. Recalled by Pharmakon Pharmaceuticals, Inc.. Units affected: 142.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 20, 2016. Severity: Moderate. Recall number: D-1290-2016.
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