PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Reported: May 31, 2017 Initiated: April 21, 2017 #Z-2127-2017
Product Description
PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Reason for Recall
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 19,043 units in total
- Distribution
- Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.
- Location
- Research Triangle Park, NC
Frequently Asked Questions
What product was recalled? ▼
PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory. Recalled by Teleflex Medical. Units affected: 19,043 units in total.
Why was this product recalled? ▼
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 31, 2017. Severity: Moderate. Recall number: Z-2127-2017.
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