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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
July 30, 2025Medical DevicesFDA
Jinan Bodor Cnc Machine Co Ltd recalls Bodor's I series laser cutting machine.
Hazard: The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).
July 30, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42 Model/Catal
Hazard: Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
July 30, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40 Model/Catal
Hazard: Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Cone with Male Tubing, Non-Locking, Ellik Evacuator. Model Number: 191-NRS. The Ellik Evacuator and adapter accessor
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Ellik Evacuator Adapter, Locking. Model Number: 190-NRS. The Ellik Evacuator and adapter accessories are compatible
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Ellik Latex Bulb, Ellik Evacuator. Model Number: 194-2. The Ellik Evacuator and adapter accessories are compatible w
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator and adapter accessories are
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter accessories are compatible w
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The reusable silicone se
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Olympus Corporation of the Americas recalls Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silicone seals fit over the b
Hazard: Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
July 30, 2025Medical DevicesFDA
Natus Neurology DBA Excel Tech., Ltd. (XLTEK) recalls Natus Brain Monitor Breakout Box, Part Number 021911; full-montage standard electroencephalograph
Hazard: Natus received two complaints of left side labeling show impedance for right side.
July 30, 2025Medical DevicesFDA
CooperSurgical, Inc. recalls Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV. Endosee System Convenience Kit with IV Tube.
Hazard: The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
July 30, 2025Medical DevicesFDA
CooperSurgical, Inc. recalls Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System Convenience Kit
Hazard: The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
July 30, 2025Medical DevicesFDA
CooperSurgical, Inc. recalls HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterog
Hazard: The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.
July 30, 2025Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion 7 M20. Fluoroscopic X-Ray System.
Hazard: Potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose.
July 30, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls SIGNA PET/MR
Hazard: GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning. As a result, acoustic levels can exceed 99dB, the limit established by International Electrotechnical Commission (IEC 60601-2-33) when using hearing protection with a Noise Reduction Rating (NRR) of 29dB, as currently required in the Operator Manual.
July 30, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls Discovery MR750w 3.0T
Hazard: GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning. As a result, acoustic levels can exceed 99dB, the limit established by International Electrotechnical Commission (IEC 60601-2-33) when using hearing protection with a Noise Reduction Rating (NRR) of 29dB, as currently required in the Operator Manual.
July 30, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls SIGNA Architect AIR
Hazard: GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning. As a result, acoustic levels can exceed 99dB, the limit established by International Electrotechnical Commission (IEC 60601-2-33) when using hearing protection with a Noise Reduction Rating (NRR) of 29dB, as currently required in the Operator Manual.
July 30, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls SIGNA Architect
Hazard: GE HealthCare has become aware that gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning. As a result, acoustic levels can exceed 99dB, the limit established by International Electrotechnical Commission (IEC 60601-2-33) when using hearing protection with a Noise Reduction Rating (NRR) of 29dB, as currently required in the Operator Manual.
July 30, 2025Medical DevicesFDA
DIGIMED CO., LTD recalls Portable X-ray system
Hazard: Some DIOX-602 units currently in use within the United States do not meet the minimum SSD requirement of 18 cm.
July 30, 2025Food & BeverageFDA
Herbalife International of America recalls Herbalife Nutrition, Relaxation Tea, Net Wt: 1.69 OZ (48g) UPC# L044KUS0A-00
Hazard: Incorrect ingredient was received from supplier and used in manufacturing finished product Relaxation Tea.
July 30, 2025Food & BeverageFDA
LLK TRADING INC recalls Needle Mushrooms, Product of China, 200 gram packages, Plastic clear packaging on top with blue on the bottom (non-trans
Hazard: Product tested positive for L. monocytogenes .
July 30, 2025Food & BeverageFDA
Gedney Foods Product, LLC recalls Gedney Ghost Pepper LIL Pickles, item 75802, Net 24 fl oz. (1.5Pts) 710mL. UPC 0 41660-00758 9. Refrigerate after o
Hazard: Products were slated for disposal due to product and container damage, but were inadvertently sold.
July 30, 2025Food & BeverageFDA
Gedney Foods Product, LLC recalls Zinger Pickle products under the following labels: 1. Gedney Zinger Chips, item 18800, 24 fl oz. (1-1/2 Pt) 710mL.
Hazard: Products were slated for disposal due to product and container damage, but were inadvertently sold.
July 30, 2025Food & BeverageFDA
Gedney Foods Product, LLC recalls Dill Pickles packaged under the following label: 1. Gedney Whole Pickles, item 15100, Net 32 fl oz. (1Qt)946mL. UPC 0
Hazard: Products were slated for disposal due to product and container damage, but were inadvertently sold.
July 30, 2025Food & BeverageFDA
MING HONG INTERNATIONAL INC. recalls Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1
Hazard: Individual consumer size Wasabi mini pack label does not declare allergen ingredient Yellow 5.
July 30, 2025Food & BeverageFDA
Mondelez Global Llc recalls Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 1
Hazard: Undeclared allergens (Peanut) due to mispackaging
July 30, 2025Food & BeverageFDA
Mondelez Global Llc recalls Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38
Hazard: Undeclared allergens (Peanut) due to mispackaging
July 30, 2025Food & BeverageFDA
Mondelez Global Llc recalls Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton.
Hazard: Undeclared allergens (Peanut) due to mispackaging