Z-2242-2013 Class II Terminated
FDA device recall Z-2242-2013 was initiated by 3M Company - Health Care Business on Aug 5, 2013 and is designated Class II. Reason for recall: 3M is conducting a voluntary product recall of selected lots of 3M" Scotchcast" Wet or Dry Cast Padding. Upon investigation of a health care provider feedback, and confirmed with internal testing… The recall status is terminated (terminated Jun 16, 2014). Affected quantity: 1207 cases (4 puches per case, 20 rolls per pouch).
Recall Details
- Product Type
- Devices
- Report Date
- Sep 25, 2013
- Initiation Date
- Aug 5, 2013
- Termination Date
- Jun 16, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1207 cases (4 puches per case, 20 rolls per pouch)
Product Description
Reason for Recall
Distribution Pattern
Worldwide Distribution - USA including AL, AZ, AR, CA, CO,CT, FL, GA, HI, IL, IN,KS,KY, LA, MD, MA, MI, MN, MO, NE, NV, NJ, NY, NC, OH, OR,PA, TN, TX, UT,VA, WA, and WI. Internationally to GERMANY, CANADA, BELGIUM, NETHERLANDS, HONG KONG, NEW ZEALAND, AUSTRALIA, INDIA, KOREA, SINGAPORE AND UNITED ARAB EMIRATES, JAPAN, JAMAICA..
Code Information
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2242-2013
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026