CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
Reported: May 6, 2020 Initiated: March 16, 2020 #Z-1822-2020
Product Description
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
Reason for Recall
The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.
Details
- Recalling Firm
- Avanos Medical, Inc.
- Units Affected
- 1766
- Distribution
- Worldwide and US Nationwide Distribution: AZ, CA, CT, FL, GA, IA, ID, IL, LA, MO, MN, MD, NY, NM, NV, NJ, OR, OK, OH, RI, TN, TX, WA, WI, ***Foreign: Distributed to Australia, Belgium, Canada, France, Germany, Ireland, Italy, Netherlands, Romania, United Arab Emirates, United Kingdom
- Location
- Alpharetta, GA
Frequently Asked Questions
What product was recalled? ▼
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit. Recalled by Avanos Medical, Inc.. Units affected: 1766.
Why was this product recalled? ▼
The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 6, 2020. Severity: Moderate. Recall number: Z-1822-2020.
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