Class I ยท High risk
Atovaquone Oral Suspension USP
Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.
National Drug Code
Is NDC 31722-0629-21 recalled?
Atovaquone · 1 BOTTLE in 1 CARTON (31722-629-21) / 210 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 31722-0629-21 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Atovaquone
- Strength
- ATOVAQUONE 750 mg/5mL
- Form
- Suspension · Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 31722-0629
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
Free recall alerts
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