Recall of Chorionic Gonadotropin Due to Sterility Assurance Concerns
Oregon Compounding Centers is recalling 145 vials of Chorionic Gonadotropin due to quality control issues affecting sterility assurance.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric for significant injury or health risk potential.
Plain-English summary
Oregon Compounding Centers, Inc. dba Creative Compounds is recalling 145 vials of Chorionic Gonadotropin, 4000 Units, sterile powder for reconstitution. The affected lots are 20140728@55 (discard date 1/14/2015) and 20140915@14 (discard date 3/8/2015). The product was distributed in Oregon and Washington.
The recall was initiated due to a lack of sterility assurance. FDA inspection identified concerns associated with quality control procedures that present a potential risk to sterility assurance for all lots of sterile products compounded by the pharmacy that are not expired.
Consumers and healthcare providers should stop using the affected product and contact the recalling firm or their healthcare provider for instructions on return or replacement.
The recalled product
- Product
- CHORIONIC GONADOTROPIN, 4000 Units, sterile powder for reconstitution, glass vial, RX, Creative Compounds, Wilsonville, OR 97070
- Hazard
- Affected units
- 145
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)
- Lot #: 20140728@55
- discard date: 1/14/2015
- Lot #: 20140915@14
- discard date: 3/8/2015.
Distribution
Part of a larger recall action
This product is one of 56 recalled by Oregon Compounding Centers, Inc. dba Creative Compounds under a single FDA (Drugs) 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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