Pneumothorax Kit
Reported: April 11, 2018 Initiated: October 24, 2017 #Z-1299-2018
Product Description
Pneumothorax Kit
Reason for Recall
Product packaging may not be completely sealed.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- N/A
- Distribution
- Nationally
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Pneumothorax Kit. Recalled by Arrow International Inc. Units affected: N/A.
Why was this product recalled? ▼
Product packaging may not be completely sealed.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 11, 2018. Severity: Moderate. Recall number: Z-1299-2018.
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