Centurion Glass Medicine Cup Recall Due to Incomplete Sterile Seals
Centurion Medical Products is recalling 600 sterile glass medicine cups because incomplete seals may compromise sterility.
The agency’s classification
FDA (Devices): 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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (compromised sterility) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
Centurion Medical Products Corporation is recalling 600 units of the Centurion-Medicine Cup GMC205, a 2-ounce sterile glass medicine cup. The recall is due to incomplete seals on the sterile package, which may compromise the sterility of the product.
The affected product is identified by the lot code GMC205 GLASS MEDICINE CUP 2 OUNCE STERILE 2019022590. The product was distributed nationwide and to Ghana.
Consumers should stop using the affected medicine cups and contact the recalling firm for further instructions.
The recalled product
- Product
- Centurion-Medicine Cup GMC205 GLASS MEDICINE CUP 2 OUNCE STERILE
- Manufacturer
- Centurion Medical Products Corporation
- Hazard
- Affected units
- 600
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 (1)
- Product-Lot Code: GMC205 GLASS MEDICINE CUP 2 OUNCE STERILE 2019022590
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 54 recalled by Centurion Medical Products Corporation under a single FDA (Devices) 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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