Medline CHEST TUBE REORDER NO: DYNJ36762A
Reported: September 14, 2022 Initiated: July 21, 2022 #Z-1683-2022
Product Description
Medline CHEST TUBE REORDER NO: DYNJ36762A
Reason for Recall
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
Details
- Recalling Firm
- Medline Industries Inc.
- Units Affected
- 300 kits
- Distribution
- U.S. Nationwide distribution in the state of AL.
- Location
- Laredo, TX
Frequently Asked Questions
What product was recalled? ▼
Medline CHEST TUBE REORDER NO: DYNJ36762A. Recalled by Medline Industries Inc.. Units affected: 300 kits.
Why was this product recalled? ▼
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 14, 2022. Severity: Moderate. Recall number: Z-1683-2022.
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