California Department of Public Health inspection at the facility found undeclared milk (from whey).
All Recalls
95,050 total recalls in our database
Young Ocean brand Seasoned Alaskan Pollock Roe is recalled because the label declares Hondashi ingredient but does not declare sub-ingredient bonito and lactose (milk).
🍎 Food Class I - Dangerous
Undeclared Pecan allergen. Bourbon Honey Pecan ice cream was packaged in a container that was labeled as Gluten Free Cookies N Cream and the lid was labeled as Bourbon Honey Pecan.
🍎 Food Class I - Dangerous
Product contains undeclared Allergens: Walnuts & Pecans
🏥 Medical Devices Class I - Dangerous
Affected products may have been manufactured with the catheter distal end hole too small
🏥 Medical Devices Class I - Dangerous
Affected products may have been manufactured with the catheter distal end hole too small
The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .
🏥 Medical Devices Class I - Dangerous
The heated tube sets were consistently leaking and detaching from the cassette.
AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero Generator PG (1) Catalog Number:12740000 UPN: H78712740000 (2) Solero Generator US PG Catalog Number: 12740000US UPN: H78712740000US0 (3) Solero Generator Service Loaner PG Catalog No: 12740000L UPN: H78712740000L0 (4) Solero Generator Service Loaner US PG Catalog Number: 12740000USL UPN: H78712740000USL0
Angiodynamics Inc. (Navilyst Medical Inc.)
🏥 Medical Devices Class I - Dangerous
Updated Warning Statements in the Operator's Manual/Directions for Use and Software Updates to reduce the risk of potential patient harm due to a delay in performing a procedure
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV28F
OriGen Biomedical
🏥 Medical Devices Class I - Dangerous
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number: 191126 - Product Usage: The 2008T hemodialysis machine is indicated for acute and chronic dialysis therapy in a healthcare facility.
Fresenius Medical Care Renal Therapies Group
🏥 Medical Devices Class I - Dangerous
Power Logic Board Fail Message on the 2008T BlueStar Machine with software version 2.72.
🏥 Medical Devices Class I - Dangerous
The OMNIBotics iBlock Cutting Guide does not lock onto the iBlock Saw Guide as intended and may loosen during use.
🏥 Medical Devices Class I - Dangerous
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
🏥 Medical Devices Class I - Dangerous
The heated tube sets were consistently leaking and detaching from the cassette.
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV19F
OriGen Biomedical
🏥 Medical Devices Class I - Dangerous
Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.
Sterile Nail Clipper Concave Edge (67710)
Centurion Medical Products
🏥 Medical Devices Class I - Dangerous
Compromised seal on the sterile barrier pouch.
🏥 Medical Devices Class I - Dangerous
Updated Warning Statements in the Operator's Manual/Directions for Use and Software Updates to reduce the risk of potential patient harm due to a delay in performing a procedure
🏥 Medical Devices Class I - Dangerous
Abnormal coloration of agar plates and the growth of non-characteristic MRSA colonies.
🏥 Medical Devices Class I - Dangerous
Affected products may have been manufactured with the catheter distal end hole too small
🏥 Medical Devices Class I - Dangerous
Affected products may have been manufactured with the catheter distal end hole too small