Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS, REF 8670009, QTY 1 EA, STERILE R, Rx only
Reported: May 17, 2017 Initiated: April 13, 2017 #Z-2047-2017
Product Description
Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS, REF 8670009, QTY 1 EA, STERILE R, Rx only
Reason for Recall
Product packaging may incorrectly include two bevel-tipped needles or two trocar-tipped needles instead of one diamond-tipped needle and one bevel-tipped needle.
Details
- Recalling Firm
- Medtronic Sofamor Danek USA Inc
- Units Affected
- 36 units
- Distribution
- US Distribution to the state of : OK and to the countries of : Italy, Germany, France , Belgium, Spain and Japan.
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS, REF 8670009, QTY 1 EA, STERILE R, Rx only. Recalled by Medtronic Sofamor Danek USA Inc. Units affected: 36 units.
Why was this product recalled? ▼
Product packaging may incorrectly include two bevel-tipped needles or two trocar-tipped needles instead of one diamond-tipped needle and one bevel-tipped needle.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 17, 2017. Severity: Moderate. Recall number: Z-2047-2017.
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