McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558
Reported: March 24, 2021 Initiated: February 9, 2021 #Z-1251-2021
Product Description
McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558
Reason for Recall
Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens
Details
- Recalling Firm
- Cardinal Health 200, LLC
- Units Affected
- 108,000 units
- Distribution
- Worldwide distribution - US Nationwide distribution and the countries of AE, Japan.
- Location
- Mansfield, MA
Frequently Asked Questions
What product was recalled? ▼
McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558. Recalled by Cardinal Health 200, LLC. Units affected: 108,000 units.
Why was this product recalled? ▼
Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 24, 2021. Severity: Moderate. Recall number: Z-1251-2021.
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