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Latest Product Recalls Today

Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.

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Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 2,026 - 2,050 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-1634-2026
Medical Device High
Apr 1, 2026 Recall: Feb 19, 2026
Details
FDA Z-1601-2026
Medical Device High
Apr 1, 2026 Recall: Jan 23, 2026
Details
Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.
FDA Z-1632-2026
Medical Device High
Apr 1, 2026 Recall: Mar 17, 2026
Details
Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
FDA Z-1611-2026
Medical Device High
Apr 1, 2026 Recall: Feb 12, 2026
Details
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property.
FDA Z-1588-2026
Medical Device High
Apr 1, 2026 Recall: Feb 18, 2026
Details
FDA Z-1579-2026
Medical Device High
Apr 1, 2026 Recall: Feb 13, 2026
Details
Philips L17-5 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
FDA Z-1621-2026
Medical Device High
Apr 1, 2026 Recall: Sep 5, 2025
Details
FDA Z-1603-2026
Medical Device High
Apr 1, 2026 Recall: Jan 23, 2026
Details
Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
FDA Z-1612-2026
Medical Device High
Apr 1, 2026 Recall: Feb 12, 2026
Details
Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion set, into a patient s subcutaneous tissue. As with current insulin infusion pumps on the U.S. market, the desired timing and quantity of the insulin delivery is programmed by the user (i.e., the patient).
The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead direct users to confirm that the infusion set is not connected to the body. Following this instruction could result in unintended insulin delivery, potentially leading to a hypoglycemic event.
FDA Z-1636-2026
Medical Device High
Apr 1, 2026 Recall: Jan 30, 2026
Details
16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
FDA Z-1577-2026
Medical Device High
Apr 1, 2026 Recall: Feb 13, 2026
Details
Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;
The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.
FDA Z-1651-2026
Medical Device High
Apr 1, 2026 Recall: Feb 11, 2026
Details
MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61
Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and 6.62), which could result in a risk of hypoglycemia or hyperglycemia due to inaccuracies in insulin delivery (either under-delivery, over-delivery, or cessation of delivery).
FDA Z-1635-2026
Medical Device High
Apr 1, 2026 Recall: Jan 30, 2026
Details
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation during an endoscopic or open surgical procedure.
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.
FDA Z-1640-2026
Medical Device High
Apr 1, 2026 Recall: Feb 25, 2026
Details
Philips OMNI II TEE Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
FDA Z-1623-2026
Medical Device High
Apr 1, 2026 Recall: Sep 5, 2025
Details
Philips X3-1 Ultrasound Transducer
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
FDA Z-1627-2026
Medical Device High
Apr 1, 2026 Recall: Sep 5, 2025
Details
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
FDA Z-1645-2026
Medical Device High
Apr 1, 2026 Recall: Feb 11, 2026
Details
FDA H-0611-2026
Food High
Apr 1, 2026 Recall: Feb 26, 2026
Details
Bulk packaged Colustrum Powder. packaged with generic product label.
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
FDA H-0602-2026
Food High
Apr 1, 2026 Recall: Aug 29, 2025
Details
FDA H-0606-2026
Food High
Apr 1, 2026 Recall: Feb 24, 2026
Details
FDA H-0609-2026
Food High
Apr 1, 2026 Recall: Feb 24, 2026
Details
Nuts.com, Espresso Malted Milk Balls, 1 lb. sealed pouch & 20 lb. clear poly bag in Nuts.com cardboard box . Packages are only sold individually .
Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
FDA H-0632-2026
Food High
Apr 1, 2026 Recall: Mar 10, 2026
Details
Doraditas de Azucar UPC 5901234123457
Gorditas and Doraditas are missing the following allergens in product label: Wheat and Soy
FDA H-0649-2026
Food High
Apr 1, 2026 Recall: Mar 6, 2026
Details
FDA H-0627-2026
Food High
Apr 1, 2026 Recall: Jan 24, 2026
Details
Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8 57919 00785 5 Distributed by: Grocery Delivery E-Services New York, NY 10005
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
FDA H-0618-2026
Food High
Apr 1, 2026 Recall: Jan 19, 2026
Details
Showing 2,026 - 2,050 of 3,321 product recalls

Product Recalls Today

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Latest Recalls By Source Agency

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CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

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Check The Publish Date First

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Prioritize High-Risk Notices

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Verify The Official Notice

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Latest Product Recalls FAQ

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Why do some recent recalls have older recall dates?

Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.

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Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.