Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.
Reported: August 26, 2015 Initiated: July 7, 2015 #Z-2388-2015
Product Description
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.
Reason for Recall
Potential breach of the sterile barrier packaging.
Details
- Recalling Firm
- C.R. Bard, Inc.
- Units Affected
- 534,972 each
- Distribution
- Nationwide Distribution-including AL, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NV, NH, NJ, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI AND DC.
- Location
- Covington, GA
Frequently Asked Questions
What product was recalled? ▼
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S. Intermittent catheter.. Recalled by C.R. Bard, Inc.. Units affected: 534,972 each.
Why was this product recalled? ▼
Potential breach of the sterile barrier packaging.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 26, 2015. Severity: Moderate. Recall number: Z-2388-2015.
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