Class II — Heritage Medical Products, Inc.
| Recalling firm | HERITAGE MEDICAL PRODUCTS, INC. |
|---|---|
| Registered facility | Heritage Medical Products, inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for bed to drop suddenly at the head while a patient is laying on it. |
| Product | 2000 Vascular with 30 Degree option |
| Quantity | 167 beds (159 US, 8 OUS) |
| Distribution | Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, OH, OK, OR, PA, SC, TX, UT, VA, WI, WY, PR. International distribution to Canada, Saudi Arabia, Trinidad & Tobago. |
| Initiated | 2016-09-02 |
| Classified | 2019-11-08 |
| Terminated | 2020-12-14 |
| Recall number | Z-0353-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Heritage Medical Products, Inc. (Z-0353-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83219/
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