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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls BD MICROBIOLOGY FLUID THIOGLYCOLLATE MED TUBE 1004321196 (100/CT) MEDIA.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls HEMOCUE INC F/GLUCOSE 201 ANALYZER (25/VL 4VL/BX) MICROCUVETTE.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT RAPID DX N AMERICA LLC CHOLESTECH LDX LIPID PROFILE+GLUCOSE (10/BX 50BX/CS) TEST.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT RAPID DX N AMERICA LLC, TEST CHOLESTEC LDXLIPID PROFILE (10/BX 50BX/CS) CASSETTES.
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT RAPID DX N AMERICA LLC MULTI ANALYTE LVL1&2250UL CHOLS CONTROL
Hazard: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
June 4, 2025Medical DevicesFDA
Maquet Cardiopulmonary Ag recalls Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital tran
Hazard: HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.
June 4, 2025Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376.
Hazard: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY Calibrator do not meet the assay Instructions for Use (IFU) reference interval due to calibrator instability resulting in increased positive bias.
June 4, 2025Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498
Hazard: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY Calibrator do not meet the assay Instructions for Use (IFU) reference interval due to calibrator instability resulting in increased positive bias.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls ELEOS COLLAR STEM, CEMENTED, FLUTED, 15MM X 120MM. Model Number: HC-15120-03M. Component of Limb Salvage System with
Hazard: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which included an implant that was 15mm in diameter (HC-15120-03M) instead of being 13mm as stated on the package. The corresponding 15mm cemented stems were mislabeled as size 13mm cemented stems.
June 4, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls ELEOS COLLAR STEM, CEMENTED, FLUTED, 13MM X 120MM. Model Number: HC-13120-03M. Component of Limb Salvage System with
Hazard: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which included an implant that was 15mm in diameter (HC-15120-03M) instead of being 13mm as stated on the package. The corresponding 15mm cemented stems were mislabeled as size 13mm cemented stems.
June 4, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E10043
Hazard: There is a potential for improper crimps on the signal wires of the actuators which could result in a loss of ability to lower the bed or the foot section of the bed.
June 4, 2025Medical DevicesFDA
Beckman Coulter Ireland, Inc. recalls Apo B Reagent, REF: OSR6143
Hazard: The product Value Assignment Sheet (VAS) is used in calibration of the device. An erroneous value was included in the VAS which has the potential to generate an incorrect APO B patient result which could exceed the total allowable error for the APO B assay (11.6%). The error results in results with a positive bias up to 42%. However, based on the mitigating factors the risk to health is considered to be negligible or limited.
June 4, 2025Food & BeverageFDA
Williams Farms Produce Sales Co., Inc. recalls Tomato 3 Count UPC 0 33383 65504 8, 10lb box, 25lb box & 60ct/2 layer box Williams Farms Repack, LLC Lodge, SC 29082
Hazard: Product may contain Salmonella.
June 4, 2025Food & BeverageFDA
Honey Heaven Wholesale Inc recalls Kraft package is labeled as Hummingbird Organic Roasted Salted Cashews, net wt. 6oz.
Hazard: Undeclared hazelnut. The Oregon Trail Mix contains visible hazelnut and was mis-labeled as Organic Roasted Salted Cashews, but the label does not declare hazelnut.
June 4, 2025Food & BeverageFDA
East CK Trading Inc. recalls President Brand Licorice Plum (8 oz., 227g)
Hazard: Contains undeclared sulfites, undeclared FD&C Yellow 6, and unapproved color: Amaranth (E123).
June 4, 2025Food & BeverageFDA
HAWAIIAN HOST CANDIES OF LA INC recalls Mauna Loa Dark Chocolate Covered Macadamias product is a snack product and packaged in 0.6oz and 4oz plastic flexible po
Hazard: Undeclared almond and cashew.
June 4, 2025DrugsFDA
EnShiShiXiangNiShangMaoYouXianGongSi recalls ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance,
Hazard: Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
June 4, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Ph
Hazard: OOS results reported for the Dissolution (by UV) test.
June 4, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured f
Hazard: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
June 4, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured
Hazard: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
June 4, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only,
Hazard: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
June 4, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC 68462-162-01), b.) 500-count bottle (NDC 68462-162-05),
Hazard: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
June 4, 2025DrugsFDA
Alembic Pharmaceuticals Limited recalls Bromfenac Ophthalmic Solution 0.09%, 1.7 mL bottle, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., B
Hazard: Failed Impurities/Degradation Specifications
June 4, 2025VehiclesNHTSA
Triple E Rv, Triple E 2025 Electrical System recall
Hazard: Overheated wiring can cause electrical arcing and increase the risk of a fire.
June 4, 2025VehiclesNHTSA
Nissan 2025 Back Over Prevention recall
Hazard: A rearview image that does not display can reduce the driver's view of what is behind the vehicle, increasing the risk of a crash.
June 3, 2025VehiclesNHTSA
Hyundai 2025 Exterior Lighting recall
Hazard: Improperly aimed headlights can result in insufficient illumination of the road, decreasing the driver's visibility and increasing the risk of a crash.
June 3, 2025VehiclesNHTSA
Ford 2023–2025 Engine recall
Hazard: An oil leak can result in loss of drive power, increasing the risk of a crash. In addition, an oil leak in the presence of an ignition source such as hot engine or exhaust components, can increase the risk of a fire.
June 3, 2025VehiclesNHTSA
Ford 2025 Service Brakes, Hydraulic recall
Hazard: Loss of brake function and wheel damage can increase the risk of a crash.
June 3, 2025VehiclesNHTSA
Rivian 2022–2025 Seat Belts recall
Hazard: An improperly secured seat belt may not restrain an occupant as intended, increasing the risk of injury during a crash.
June 3, 2025VehiclesNHTSA
Mazda 2024–2025 Electronic Stability Control (Esc) recall
Hazard: An indicator light that does not illuminate may fail to warn the driver of a TCS or DSC system issue, increasing the risk of a crash.