Teleflex Recalls Certain Arrow Peripheral Catheter System Citing Risk Of Separation, Leakage
Portfolio Pulse from Vandana Singh
Teleflex Incorporated and its subsidiary Arrow International are recalling the ARROW Endurance Extended Dwell Peripheral Catheter System due to reports of catheter separation or leakage. The FDA has classified this as a Class I recall, the most serious type of recall. Teleflex/Arrow International has received 83 complaints, 18 reported injuries, and no deaths.
June 26, 2023 | 6:17 pm
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Teleflex recalls its ARROW Endurance Extended Dwell Peripheral Catheter System due to risks of separation and leakage. The FDA has classified this as a Class I recall, with 83 complaints and 18 reported injuries.
The recall of Teleflex's ARROW Endurance Extended Dwell Peripheral Catheter System is a significant event for the company, as it is classified as a Class I recall by the FDA, indicating a high risk of serious injury or death. This could negatively impact the company's reputation, sales, and stock price in the short term.
CONFIDENCE 90
IMPORTANCE 80
RELEVANCE 100