Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
Reported: July 31, 2019 Initiated: April 30, 2019 #Z-2052-2019
Product Description
Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389
Reason for Recall
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Details
- Recalling Firm
- Cardinal Health 200, LLC
- Units Affected
- N/A
- Distribution
- Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL
- Location
- Mansfield, MA
Frequently Asked Questions
What product was recalled? ▼
Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389. Recalled by Cardinal Health 200, LLC. Units affected: N/A.
Why was this product recalled? ▼
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 31, 2019. Severity: Moderate. Recall number: Z-2052-2019.
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