PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Reported: May 20, 2020 Initiated: March 17, 2020 #Z-1946-2020
Product Description
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Reason for Recall
Iincorrectly packaged without the required lidocaine as labeled
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 655 kits
- Distribution
- AZ, CT, GA, IL, LA, MA, MI, MN, ND, NE, NY, OH, SD, TX),
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D. Recalled by Becton Dickinson & Company. Units affected: 655 kits.
Why was this product recalled? ▼
Iincorrectly packaged without the required lidocaine as labeled
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 20, 2020. Severity: Moderate. Recall number: Z-1946-2020.
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