FDA Recall Open, Classified

Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C

Recall: Z-1381-2024 · Initiated February 16, 2024

Recall

Recall Number
Z-1381-2024
Event Number
94030
Firm
Medivance Inc.
FEI Number
3003329224
Product Code
DWJ
Status
Open, Classified
Root Cause
Process control
Initiated
February 16, 2024
Posted
March 26, 2024
Address
321 S Taylor Ave, Unit 200, Louisville, CO, 80027-3600

Description

Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C

Reason

Neonatal pads are experiencing reduced water flow, which may reduce or prevent water heating or cooling performance of the pads that are part of a temperature management system.

Action

On 2/16/24, BD mailed or emailed recall notices to customers who were asked to do the following: 1) Immediately Discontinue Use 2) Immediately quarantine affected pads, record your inventory totals on the Customer Response Form, discard all devices within your facility's control per your facility's procedures. 3) Share this notice with any users of the product within your facilities or with any facility affected product was distributed to. 4) Complete and return the attached Customer Response Form to the BD contact noted on the form. If you require further assistance contact BD Customer Support at 1-844-823-5433. Say "Recall" when prompted M-F 8am -5pm CT.

Distribution

Worldwide - US Nationwide distribution including in the states of IL, AL, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Belgium, Australia, Singapore, South Korea, Taiwan, Japan, China, Thailand.

Quantity

1,654