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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.

Find Recent Product Recall Alerts

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 1,626 - 1,650 of 3,321 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-1893-2026
Medical Device High
Apr 29, 2026 Recall: Mar 13, 2026
Details
FDA Z-1892-2026
Medical Device High
Apr 29, 2026 Recall: Feb 27, 2026
Details
Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
X-Ray generator may malfunction resulting in the X-Ray being inoperable.
FDA Z-1918-2026
Medical Device High
Apr 29, 2026 Recall: Mar 27, 2026
Details
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
FDA Z-1920-2026
Medical Device High
Apr 29, 2026 Recall: Mar 11, 2026
Details
FDA Z-1886-2026
Medical Device High
Apr 29, 2026 Recall: Feb 27, 2026
Details
Medline Kits: 1) ENT PACK, Model Number: DYNJ59030B; 2) ENT, Model Number: DYNJ908586C; 3) LH 3 PORT W/O WASTEBAG, Model Number: VASC1081C
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
FDA Z-1839-2026
Medical Device High
Apr 29, 2026 Recall: Feb 25, 2026
Details
Flamingo Funnel Small, Model Number SQ20012-01
Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.
FDA Z-1924-2026
Medical Device High
Apr 29, 2026 Recall: Mar 16, 2026
Details
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
FDA Z-1901-2026
Medical Device High
Apr 29, 2026 Recall: Mar 25, 2026
Details
FDA Z-1836-2026
Medical Device High
Apr 29, 2026 Recall: Feb 25, 2026
Details
Medline Kits: 1) HYSTEROSCOPY PACK, Model Number: DYNJ48399C; 2) SLING PACK, Model Number: DYNJ62849B
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
FDA Z-1847-2026
Medical Device High
Apr 29, 2026 Recall: Feb 25, 2026
Details
Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.: 10714002; Product/UPN No.: H787107140025 (Box), H787107140020 (Pouch); Box Quantity: 10 pouches;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
FDA Z-1859-2026
Medical Device High
Apr 29, 2026 Recall: Mar 3, 2026
Details
LeadCare¿ Plus Blood Lead Test Kit; Catalog Number: 82-0004; The LeadCare¿ Plus kit is provided with the following materials: " Sensors (4 containers of 24 each; 96 tests) " Treatment Reagent Tubes (4 packages of 24 each; 96 tests) " Calibration Button (1 @) " Lead Control Level 1 (1 @ 2 mL) " Lead Control Level 2 (1 @ 2 mL)
Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test Systems. False positive lead results may cause delayed results and additional unnecessary testing.
FDA Z-1894-2026
Medical Device High
Apr 29, 2026 Recall: Mar 13, 2026
Details
AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box), H787137090050 (Pouch); Box Quantity: 5 pouches;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
FDA Z-1872-2026
Medical Device High
Apr 29, 2026 Recall: Mar 3, 2026
Details
FDA Z-1916-2026
Medical Device High
Apr 29, 2026 Recall: Mar 11, 2026
Details
FDA Z-1876-2026
Medical Device High
Apr 29, 2026 Recall: Feb 27, 2026
Details
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.
Potential for detachment of a distal tip component of the device during use.
FDA Z-1851-2026
Medical Device High
Apr 29, 2026 Recall: Mar 23, 2026
Details
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Quantity: 5 pouches;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
FDA Z-1866-2026
Medical Device High
Apr 29, 2026 Recall: Mar 3, 2026
Details
FDA Z-1883-2026
Medical Device High
Apr 29, 2026 Recall: Feb 27, 2026
Details
LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
FDA Z-1930-2026
Medical Device High
Apr 29, 2026 Recall: Mar 9, 2026
Details
Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Product/UPN No.: H787107140165 (Box), H787107140160 (Pouch); Box Quantity: 5 pouches;
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
FDA Z-1863-2026
Medical Device High
Apr 29, 2026 Recall: Mar 3, 2026
Details
FDA Z-1884-2026
Medical Device High
Apr 29, 2026 Recall: Feb 27, 2026
Details
FDA Z-1834-2026
Medical Device High
Apr 29, 2026 Recall: Feb 25, 2026
Details
FDA Z-1835-2026
Medical Device High
Apr 29, 2026 Recall: Feb 25, 2026
Details
LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
FDA Z-1933-2026
Medical Device High
Apr 29, 2026 Recall: Mar 9, 2026
Details
FDA Z-1903-2026
Medical Device High
Apr 29, 2026 Recall: Mar 25, 2026
Details
Showing 1,626 - 1,650 of 3,321 product recalls

Product Recalls Today

Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.

Recent Product Recall Alerts

Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.

High-Risk Recall Updates

High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.

Daily Official Source Coverage

This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.

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.

How To Use The Latest Product Recalls Page

Check The Publish Date First

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Filter By Product Type

Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.

Prioritize High-Risk Notices

Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.

Verify The Official Notice

Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.

Latest Product Recalls FAQ

Helpful context for searches such as product recalls today, recent product recalls and recall alerts.

How often is the latest product recall list updated?

The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.

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.

What should I check on a recent food recall?

Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.

Can I get only high-risk recalls?

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