3M Scotchcast — Class II medical device recall Z-2242-2013
Terminated recall by 3M Company - Health Care Business, reported 2013-09-25, distributed in AL, AR, AZ, CA, CO, CT, FL, GA…. 3M is conducting a voluntary product recall of selected lots of 3M" Scotchcast" Wet or Dry Cast Padding. Upon
| Recall number | Z-2242-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company - Health Care Business, Saint Paul, MN, United States |
| Recall initiated | 2013-08-05 |
| Classified | 2013-09-18 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2014-06-16 |
| Distributed | AL, AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NE, NJ, NV, NY, OH, OR, PA, TN, TX, UT, VA, WA, WI |
| Countries outside the US | AE, AU, BE, CA, DE, HK, IN, JM, JP, KR, NL, NZ, SG |
| Lot numbers | 792920, 792921, 792922, 792923, 793090, 793098, 793116, 793636, 793637, 793638, 793640, 796077, 796078, 796079, 798487, 798488, 798489, 799235, 799236, WDP2, WDP3, WDP4, WDP6 |
| Model numbers | WDP2, WDP3, WDP4, WDP6 |
Product
3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing casts for either wet or dry immobilization.
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, it was found that the cast padding material does not consistently repel water. Lack of repellency may result in prolonged cast dry times after exposure to wet conditions. There have been no repo
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2242-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.