Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
Reported: June 15, 2016 Initiated: March 25, 2016 #Z-1936-2016
Product Description
Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
Reason for Recall
BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm x 25 mm) and Henry Schein 10 mL Single Use Syringe Luer-Lock are being recalled due to possible adulteration and non-conforming manufacturing practices.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 176,000 units
- Distribution
- Nationwide Distribution to NY only
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection. Recalled by Becton Dickinson & Company. Units affected: 176,000 units.
Why was this product recalled? ▼
BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm x 25 mm) and Henry Schein 10 mL Single Use Syringe Luer-Lock are being recalled due to possible adulteration and non-conforming manufacturing practices.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 15, 2016. Severity: Moderate. Recall number: Z-1936-2016.
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