SunMed Tracheal Tube Recalled Due to Suction Catheter Passage Issues
Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.
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 does not report any illnesses, injuries, or hospitalizations, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes, Size 2.5, Model Number 1-7333-25. The recall was initiated because a 6Fr suction catheter could not pass through the samples smoothly.
The affected units were distributed nationwide in the state of Michigan. The recall covers 27,200 units across multiple lot numbers.
Consumers should stop using the affected tracheal tubes and contact the recalling firm for further instructions.
The recalled product
- Product
- SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
- Manufacturer
- WELL LEAD MEDICAL CO. LTD
- Category
- Medical Device — Tracheal Tubes
- Hazard
- Affected units
- 27,200
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 (20)
- Model Number: 1-7333-25
- UDI-DI:10889483048108
- Lot No.: 2108011462
- 2108011506
- 2109011963
- 2111012039
- 2112012040
- 2204010568
- 2204010569
- 2204010734
- 2205010833
- 2207011263
- 2208011729
- 2208011789
- 2304010830
- 2306011372
- 2306011425
- 2308011907
- 2308012011
- 2308012012
Distribution
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