Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(1) Carefusion V. Mueller Graves Vaginal Speculum Recalled by Carefusion 2200 Inc Due to A portion of the two products were incorrectly...
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 Carefusion 2200 Inc directly.
Affected Products
(1) Carefusion V. Mueller Graves Vaginal Speculum, Catalog #GL11, Medium Blade, 4 x 1 3/8" (10.2 X 3.5cm); and (2) Carefusion V. Mueller Pederson Vaginal Specula, Catalog #GL31, Medium, 4 x 7/8" (10.2 x 2.2cm).
Quantity: 726 units
Why Was This Recalled?
A portion of the two products were incorrectly marked (etched) and packaged resulting in a product mismatch. The labels and laser etchings were switched on the two products.
Where Was This Sold?
This product was distributed to 35 states: AL, AZ, AR, CA, CO, CT, FL, HI, IL, IN, IA, KY, LA, MD, MA, MI, MN, MO, MT, NE, NV, NJ, NM, NY, NC, OH, OR, PA, SC, TN, TX, VA, WA, WV, WI
About Carefusion 2200 Inc
Carefusion 2200 Inc has 112 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report