Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer Recalled by Zimmer Surgical Inc Due to Devices were placed in a shipper carton without...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Surgical Inc directly.
Affected Products
Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer Surgical, Inc. Intended for post-operative collection of wound drainage.
Quantity: 36 units
Why Was This Recalled?
Devices were placed in a shipper carton without the appropriate number of the Instructions for Use (IFU). Packaging specifications require that each sales unit is accompanied by an IFU. Only one IFU was present in the shipper carton, instead of one IFU per each of the two sales units.
Where Was This Sold?
This product was distributed to 8 states: AZ, CA, ID, IL, MD, NC, RI, SC
About Zimmer Surgical Inc
Zimmer Surgical Inc has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report