Recall Z-0756-2017— Covidien LLC
Class II · Terminated
Class II FDA medical device recall by Covidien LLC, initiated 2016-10-14, terminated 2018-08-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Covidien Precision Specimen Container- 4 oz (118 mL), Plastic Screw Top Cap, OR Packaged, Sterile Item Code: 17099. Reason: Sterility of the outer surface of the container compromised due to packaging defect..
- Recalling firm
- Covidien LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-10-14
- Terminated
- 2018-08-08
- Firm location
- North Haven, CT, United States
Product description
Covidien Precision Specimen Container- 4 oz (118 mL), Plastic Screw Top Cap, OR Packaged, Sterile Item Code: 17099
Reason for recall
Sterility of the outer surface of the container compromised due to packaging defect.
Data sourced from openFDA. This site is unofficial and independent of the FDA.