PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Reported: November 6, 2019 Initiated: July 15, 2019 #Z-0256-2020
Product Description
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Reason for Recall
Supplier initiated recall of the GRIPPER Needles
Details
- Recalling Firm
- Centurion Medical Products Corporation
- Units Affected
- 200 kits
- Distribution
- IL
- Location
- Williamston, MI
Frequently Asked Questions
What product was recalled? ▼
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817. Recalled by Centurion Medical Products Corporation. Units affected: 200 kits.
Why was this product recalled? ▼
Supplier initiated recall of the GRIPPER Needles
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 6, 2019. Severity: Moderate. Recall number: Z-0256-2020.
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