Cook Inc. Recalls Rosen Curved Wire Guides Due to Labeling Error
Cook Inc. is recalling Rosen Curved Wire Guides because the labels fail to state that the product is heparin-coated.
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 identifies the issue as a labeling omission regarding heparin coating without reporting any illnesses or injuries, fitting the criteria for a moderate severity labeling error.
Plain-English summary
Cook Inc. is recalling 98,502 units of Rosen Curved Wire Guides. The recall was initiated because the product labels do not state that the device is heparin-coated.
The affected products were distributed nationally. The recall includes items with Catalog # TDW-/-SGH-BH and lot codes ranging from 3733552 to 6175191, F3729974 to F4923948, and NS4927345 to NS6177894.
Healthcare providers and consumers should check their inventory for these specific lot codes. If the product is found, it should be removed from use and returned to the manufacturer or supplier for credit or replacement.
The recalled product
- Product
- Rosen Curved Wire Guide
- Manufacturer
- Cook Inc.
- Hazard
- Affected units
- 98,502
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 20 recalled by Cook Inc. 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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