Terumo Recalls Glidesheath Introducer Sheaths Due to Packaging Seal Defect
Terumo Medical Corp is recalling specific lots of Glidesheath Introducer Sheaths because an incomplete seal may compromise sterility.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text indicates a very low defect rate (0.01%) and does not report any illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Terumo Medical Corp is voluntarily recalling specific lots of Glidesheath Slender Hydrophilic Coated Introducer Sheaths. The recall involves 7FR - 10CM (0.021) units with product code RM*RS7F10PA. The affected lots are 161109, 161216, 170118, and 170126. These products were distributed nationwide and in Canada.
The recall was initiated because an incomplete seal was detected at the chevron end of the primary packaging in a small quantity of the affected lot population. This defect affects 0.01% (1 in 10,000 units) of the population. The breach of the sterile barrier may compromise the sterility of the sheath.
Healthcare providers and facilities should check their inventory for the specific lot numbers listed above. If the affected products are found, they should be removed from use and returned to Terumo Medical Corp or the distributor.
The recalled product
- Product
- Glidesheath Slender Hydrophilic Coated Introducer Sheath, 7FR - 10CM (0.021), REF/Product Code RM*RS7F10PA, STERILE, Rx ONLY
- Manufacturer
- Terumo Medical Corp
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 s 161109
- 161216
- 170118
- 170126
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 17 recalled by Terumo Medical Corp 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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