PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.
Reported: July 15, 2020 Initiated: June 11, 2020 #Z-2499-2020
Product Description
PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.
Reason for Recall
Smiths Medical became aware that one (1) lot of PORT-A-CATH¿ II POWER P.A.C. Low Profile" System (SKU 21-4477-24) was packaged with an 8Fr catheter instead of a 6Fr catheter.
Details
- Recalling Firm
- Smiths Medical ASD Inc.
- Units Affected
- 46 kits
- Distribution
- Domestic Distribution: AR, CT, MS,TN,TX
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.. Recalled by Smiths Medical ASD Inc.. Units affected: 46 kits.
Why was this product recalled? ▼
Smiths Medical became aware that one (1) lot of PORT-A-CATH¿ II POWER P.A.C. Low Profile" System (SKU 21-4477-24) was packaged with an 8Fr catheter instead of a 6Fr catheter.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 15, 2020. Severity: Moderate. Recall number: Z-2499-2020.
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