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FDA (Device enforcement)Recalled 2020-11-18closedclass ii

Becton Dickinson & Company: BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of

Is my product affected?

BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.

  • UPC 30382903051060

Check against the official notice below — it lists the full affected range.

What happened

Becton Dickinson & Company has recalled BD PrecisionGlide Needle 30G x 1/2 (catalog reference 305106, lot number 9128897) due to the confirmed presence of blood on the needle cannulas. This contamination poses a possible infection risk if the blood goes unnoticed before a clinician uses the needle. Approximately 1.43 million units were distributed worldwide, including throughout the United States and in Canada, China, and Singapore. The affected product has an expiration date of June 30, 2024.

The source record does not specify a remedy or recommended action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 9128897. The possibility of infection may be present if the blood is not noticed prior to use by the clinician.

Details from the source

Reason for recall: BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 9128897. The possibility of infection may be present if the blood is not noticed prior to use by the clinician. Distribution: Worldwide distribution - US Nationwide distribution including in the states of CA, CT, FL, IL, KY, MO, NJ, NY, OH, PA, PR, SC, TN, VA and the countries of Canada, China, Singapore. Quantity: 1,430,000 Lot/code info: Catalog Ref No.: 305106 Lot No:. 9128897 Expiration Date: 2024-06-30 UDI: 30382903051060 Product Package Size: 100 units per carton

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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