BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Reported: November 6, 2019 Initiated: March 7, 2019 #Z-0252-2020
Product Description
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Reason for Recall
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 2,624,160 (2,169,703 US; 454,457 OUS)
- Distribution
- Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan.
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608. Recalled by Becton Dickinson & Company. Units affected: 2,624,160 (2,169,703 US; 454,457 OUS).
Why was this product recalled? ▼
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 6, 2019. Severity: Moderate. Recall number: Z-0252-2020.
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