FDAJanuary 3, 2018device
HEMASHIELD Knitted Double Velour Cardiovascular Fabric
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
A probable mislabeling of the product: a different-sized product is referenced on the product packaging label (i.e. 2.5 cm (width) x 7.6 cm (length)) while the actual product inside the box is 2.5 cm (width) x 15 cm (length).
What to do
FDA enforcement status: Terminated
Brands named
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UPCs
00384401017899
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCJC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries2026-04-16
- FDAThe product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.2025-08-29
- FDAGetinge 88-Series Washer- Disinfector. Model Number: 88-5.2025-08-29
- FDATomato 3 Count UPC 0 33383 65504 8, 10lb box, 25lb box & 60ct/2 layer box Williams Farms Repack, LLC Lodge, SC 290822025-04-30
- FDAWasher Disinfector Aquadis 56; Model Number: 56A2025-04-02
- FDAWasher Disinfector Aquadis 56; Model Number: 56M2025-04-02
- FDAVaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.2025-01-15
- FDAMEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 710001B02024-10-03
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