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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
January 14, 2026Medical DevicesFDA
Sophysa recalls The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor
Hazard: Customer complaints of Pressio monitor rebooting.
January 14, 2026Medical DevicesFDA
CareFusion 303, Inc. recalls BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,
Hazard: Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
January 14, 2026Medical DevicesFDA
Remote Diagnostic Technologies Ltd. recalls Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel
Hazard: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If healthcare providers base clinical judgment on unvalidated measurements, this could potentially lead to incorrect clinical decisions.
January 14, 2026Medical DevicesFDA
Beckman Coulter, Inc. recalls Beckman Coulter UniCel Dxl 800, Part numbers: 973100, A71456, A71457, A25288; Immunoassay Method, Troponin Subunit
Hazard: Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.
January 14, 2026Medical DevicesFDA
Beckman Coulter, Inc. recalls Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260; Immunoassay Method, Troponin Subunit
Hazard: Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.
January 14, 2026Medical DevicesFDA
Meridian Bioscience Inc recalls Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300
Hazard: The affected lots show a decline in performance over time, which may lead to false-negative results.
January 14, 2026Medical DevicesFDA
Applied Medical Resources Corp recalls Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Hazard: There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
January 14, 2026Medical DevicesFDA
Roche Diagnostics Operations, Inc. recalls The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and el
Hazard: Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment.
January 14, 2026Medical DevicesFDA
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT
Hazard: Potential for incomplete scan due to unstable connection inside of floating sensor.
January 14, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Hazard: Devices are not suitable for organ transplant.
January 14, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Hazard: Devices are not suitable for organ transplant.
January 14, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
Hazard: Devices are not suitable for organ transplant.
January 14, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Hazard: A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.
January 14, 2026Medical DevicesFDA
Vision RT Ltd recalls The AlignRT InBore system contains six Class 1 lasers which enables the system s cameras to track the patient s position
Hazard: Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted from the Instructions for Use for the subject system as required by 21 CFR 1040,10(h), via conformance with recognized consensus standard IEC 60825-1 Ed. 3 (FDA Laser Notice 56).
January 14, 2026Food & BeverageFDA
South Asian Food Inc. recalls Bengal King Jhal Chanachur food treats 12.34oz (350gm)
Hazard: Contains undeclared peanuts
January 14, 2026Food & BeverageFDA
Meijer Inc recalls Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC 041250841197,
Hazard: Floating black foreign substance in the product
January 14, 2026Food & BeverageFDA
MAYEJ COMERCIALIZADORA S. de R.L. de C.V. recalls Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
Hazard: pathogen Cyclospora cayetanensis
January 14, 2026Food & BeverageFDA
GBC Food Services, LLC recalls EverRoast Chicken Caesar Wrap 85004224455 Net Wt: 11.25 oz (303g)
Hazard: Potential presence of Listeria monocytogenes.
January 14, 2026Food & BeverageFDA
GBC Food Services, LLC recalls EverRoast Chicken Caesar Salad 850042244142 Net Wt: 8.5 oz (255g)
Hazard: Potential presence of Listeria monocytogenes.
January 14, 2026Food & BeverageFDA
DIRECT SOURCE SEAFOOD LLC recalls MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel shell on 26/30 count per pound. Net 16oz. Product is packa
Hazard: Shrimp may be contaminated with Cesium-137 (Cs-137).
January 14, 2026Food & BeverageFDA
DIRECT SOURCE SEAFOOD LLC recalls waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Produc
Hazard: Shrimp may be contaminated with Cesium-137 (Cs-137).
January 14, 2026Food & BeverageFDA
ZIYAD BROTHERS IMPORTING recalls Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 retail units per wholesale case
Hazard: May contain partially hydrogenated oils
January 14, 2026Food & BeverageFDA
ZIYAD BROTHERS IMPORTING recalls Baraka French Style Puff Pastry 1lb and 1.5lbs sizes, UPCs 8 22514 28540 3 and 8 22514 28550 2, both sizes 12 retail uni
Hazard: May contain partially hydrogenated oils
January 14, 2026Food & BeverageFDA
McCain Foods USA Inc recalls Sysco Imperial Potato Tater Barrel, item number 1000006067. Frozen potato product is packaged in 6/5 lb. clear unlabeled
Hazard: Clear hard plastic fragments.
January 14, 2026Food & BeverageFDA
McCain Foods USA Inc recalls Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag
Hazard: Clear hard plastic fragments.
January 14, 2026Food & BeverageFDA
Ambriola Co., Inc., The recalls Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case
Hazard: Product tested positive for Listeria Monocytogenes.
January 14, 2026Food & BeverageFDA
Ambriola Co., Inc., The recalls Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
Hazard: Product tested positive for Listeria Monocytogenes.
January 14, 2026Food & BeverageFDA
Ambriola Co., Inc., The recalls Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)
Hazard: Product tested positive for Listeria Monocytogenes.
January 14, 2026Food & BeverageFDA
Ambriola Co., Inc., The recalls Sam's Pecorino Romano grated, 1.5 lb Plastic Bags, 12 units per case
Hazard: Product tested positive for Listeria Monocytogenes.
January 14, 2026Food & BeverageFDA
Ambriola Co., Inc., The recalls Boar's Head Grated Pecorino Romano, 6 oz Plastic Cup & Lid, 12 units per case
Hazard: Product tested positive for Listeria Monocytogenes.