Terumo Sur-vet Needle Recall Due to Potential Loss of Package Integrity
Terumo Medical Corporation is recalling 729,000 Sur-vet Needles because a potential loss of package integrity may compromise the sterility of the product.
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, and the source text describes a potential loss of package integrity that may compromise sterility without reporting specific injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Terumo Medical Corporation is recalling 729,000 units of Terumo Sur-vet Needle, 20G x 1", Product Code 100204. The recall involves Lot Numbers 180709C and 180915C. The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.
The recall is being conducted because there is a potential for a loss of package integrity that may compromise the sterility of the product. This is classified as a Class II recall by the U.S. Food and Drug Administration.
Healthcare providers and consumers should stop using the affected needles and contact Terumo Medical Corporation for further instructions or a replacement.
The recalled product
- Product
- Terumo Sur-vet Needle, 20G x 1", Product Code 100204
- Manufacturer
- Terumo Medical Corporation
- Category
- Medical Device — Needles
- Affected units
- 729,000
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 (2)
- Lot Numbers 180709C
- 180915C
Distribution
Part of a larger recall action
This product is one of 9 recalled by Terumo Medical 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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