Rugby Cerovite Liquid Recalled for Possible B. cepacia Contamination
The Harvard Drug Group is voluntarily recalling Rugby Cerovite Liquid due to possible B. cepacia contamination, which may cause serious infections in vulnerable patients.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class II, and the source text explicitly states the contamination may result in serious infections that could be life-threatening, meeting the criteria for a Severe rating.
Plain-English summary
The Harvard Drug Group, along with distribution firms Leader Brand and Major Pharmaceuticals, is voluntarily recalling Rugby Cerovite Liquid, 8 oz. (236ML). The recall affects 65,611 units of the product, identified by UPC Number 00536-2790-59, across all unexpired lots.
The recall was initiated due to possible product contamination with B. cepacia. This contamination may result in serious infections that could be life-threatening in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis.
The product was distributed nationwide in the United States. Consumers should check their inventory for the specific product and UPC number listed above. If they possess the recalled product, they should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Rugby Cerovite Liquid, 8 oz. 236ML
- Manufacturer
- The Harvard Drug Group
- Category
- Drug — Supplement
- Affected units
- 65,611
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Rugby Cerovite Liquid
- 236ML
- UPC Number: 00536-2790-59
- All Unexpired Lots
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 17 recalled by The Harvard Drug Group under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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