Medical DeviceAug 20, 2025
EMPOWR 3D KNEE INS, 4L 16MM, VE recall — FDA Z-2285-2025
Knee implants contain incorrect labeling (size and/or side incorrect)
Class IIFDA: OngoingEncore Medical, LP
August 2025 recalls — page 4
These records include useful source details for the selected month.
Medical DeviceAug 20, 2025
Ultra IABP Catheter Kit recall — FDA Z-2298-2025
Device contains indications for use and device compatibility claims that have not be reviewed and approved for safety and effectiveness by the FDA. Instructions for use are not consistent…
Class IIFDA: TerminatedInsightra Medical Inc.
Medical DeviceAug 20, 2025
GE Medical Systems GE SIGNA Premier XT (China Only), Nuclear Magnetic Resonance Imaging recall — FDA Z-2313-2025
GE HealthCare has become aware that for certain MR systems (SIGNA Artist, SIGNA Voyager, Discovery MR450 1.5T, Optima MR450w 1.5T, SIGNA Architect, SIGNA Premier, SIGNA UHP, Discovery MR750…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceAug 20, 2025
Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS recall — FDA Z-2173-2025
Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large volume pump (LVP) due to the potential for underinfusion when transitioning from a flow rate to a higher flow…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceAug 20, 2025
PERLA ¿ TL MIS CANNULATED FENESTRATED POLYAXIAL SCREW recall — FDA Z-2280-2025
Cannulated fenestrated polyaxial screws may be incorrectly labeled
Class IIFDA: OngoingSPINEART SA
Medical DeviceAug 20, 2025
Diversatek Healthcare Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10 recall — FDA Z-2324-2025
Anorectal manometry procedure kit outer kit label is mislabeled with an incorrect expiration date; the manufacturing date was used in place of the expiration date. All inner labels on kit…
Class IIIFDA: OngoingDiversatek Healthcare
Medical DeviceAug 20, 2025
GE Medical Systems GE SIGNA Premier Elite (China Only), Nuclear Magnetic Resonance Imaging recall — FDA Z-2314-2025
GE HealthCare has become aware that for certain MR systems (SIGNA Artist, SIGNA Voyager, Discovery MR450 1.5T, Optima MR450w 1.5T, SIGNA Architect, SIGNA Premier, SIGNA UHP, Discovery MR750…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceAug 20, 2025
GE Medical Systems GE Signa Artist, Nuclear Magnetic Resonance Imaging System recall — FDA Z-2299-2025
GE HealthCare has become aware that for certain MR systems (SIGNA Artist, SIGNA Voyager, Discovery MR450 1.5T, Optima MR450w 1.5T, SIGNA Architect, SIGNA Premier, SIGNA UHP, Discovery MR750…
Class IIFDA: OngoingGE Medical Systems, LLC
FoodAug 20, 2025
Reser's Fine Foods Sysco Classic Tuna Salad, Reorder #6724249, net wt recall — FDA H-0543-2025
Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
Class IFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 20, 2025
The Bonami Baking Company Whole Grain Par Baked Jalapeno Cheddar Bagel --- Ingredient recall — FDA H-0487-2025
Undeclared milk from Contains statement.
Class IIFDA: OngoingThe Bonami Baking Company, Inc.
FoodAug 20, 2025
Jayone Foods Frozen Oyster Meat recall — FDA H-0500-2025
Frozen Oyster product is potentially contaminated with Norovirus
Class IIFDA: TerminatedJayone Foods, Inc.
FoodAug 20, 2025
QST Ingredients and Packaging BBQ Riblet Seasoning recall — FDA H-0496-2025
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Class IIFDA: TerminatedQST Ingredients and Packaging
FoodAug 20, 2025
Reser's Fine Foods net wt recall — FDA H-0540-2025
Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
Class IFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 20, 2025
Reser's Fine Foods Sysco Imperial Deluxe Tuna Salad, Reorder #6526826, net wt recall — FDA H-0542-2025
Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
Class IFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 20, 2025
GMP Laboratories of Lithium Orotate 2.5 recall — FDA H-0447-2025
Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
Class IIIFDA: TerminatedGMP Laboratories of America Inc
FoodAug 20, 2025
Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Sukhi's CLASSIC CURRY PASTE, Net Wt recall — FDA H-0449-2025
Potential contamination with foreign objects (metal pieces).
Class IIFDA: TerminatedJagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian…
FoodAug 20, 2025
Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Sukhi's, CLASSIC CURRY INDIAN CURRY SAUCE recall — FDA H-0451-2025
Potential contamination with foreign objects (metal pieces).
Class IIFDA: TerminatedJagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian…
FoodAug 20, 2025
The Bonami Baking Company Wheat Hamburger Buns --- Ingredient Declaration: Water, Whole recall — FDA H-0489-2025
Undeclared milk and/or eggs from sub-ingredients and/or Contains statement.
Class IIFDA: OngoingThe Bonami Baking Company, Inc.
FoodAug 20, 2025
QST Ingredients and Packaging Cajun Seasoning recall — FDA H-0498-2025
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Class IIFDA: TerminatedQST Ingredients and Packaging
FoodAug 20, 2025
The Bonami Baking Company Whole Wheat Chocolate Croissants --- Ingredients: Whole White recall — FDA H-0488-2025
Undeclared milk and soy (from soy lecithin) from sub-ingredients.
Class IIFDA: OngoingThe Bonami Baking Company, Inc.
FoodAug 20, 2025
Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Sukhi's TIKKA MASALA CURRY PASTE, Net Wt recall — FDA H-0450-2025
Potential contamination with foreign objects (metal pieces).
Class IIFDA: TerminatedJagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian…
FoodAug 20, 2025
QST Ingredients and Packaging Lemon Pepper Seasoning recall — FDA H-0497-2025
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Class IIFDA: TerminatedQST Ingredients and Packaging
FoodAug 20, 2025
Dollar General Clover Valley Instant Coffee, NET WT 8 OZ recall — FDA H-0499-2025
Potential presence of glass pieces
Class IIFDA: TerminatedDollar General Corporation
FoodAug 20, 2025
Shang Hao Jia Soda Biscuit recall — FDA H-0453-2025
Various snack cracker products are mislabeled and do not declare all allergen ingredients (Whole Milk Powder and wheat).
Class IIIFDA: TerminatedShang Hao Jia, Inc
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.