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 List
Showing 1,026 - 1,050 of 3,321 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
FDA
H-0844-2026
|
Food | High |
May 27, 2026
Recall: Apr 26, 2026
|
Details | |
|
Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case
potential presence of Salmonella
|
FDA
H-0835-2026
|
Food | High |
May 27, 2026
Recall: May 5, 2026
|
Details |
|
Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
|
FDA
H-0814-2026
|
Food | High |
May 27, 2026
Recall: Apr 22, 2026
|
Details |
|
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
|
FDA
Z-2202-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 8, 2026
|
Details |
|
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2215-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption with the potential for the patient to receive less infusion solution than intended. Exposure of hazardous substances to the patient, caregiver, or pharmacy technician is possible.
|
FDA
Z-2210-2026
|
Medical Device | High |
May 27, 2026
Recall: Mar 24, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2220-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20 Biplane OR Table (722025), Allura Xper FD20/10 (722029), Allura Xper FD20/15 (722058), Allura Xper FD20/15 OR Table (722059), Allura Xper FD20/20 (722038), Allura Xper FD20/20 OR Table (722039), Cardio Vascular-Allura (722400);
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
|
FDA
Z-2228-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 28, 2026
|
Details |
|
Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV Cesar-Powerpack (722030), Integris H5000 C / Allura 9C (722016);
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
|
FDA
Z-2229-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 28, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2222-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
|
FDA
Z-2209-2026
|
Medical Device | High |
May 27, 2026
Recall: Mar 23, 2026
|
Details |
|
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624
Due to stain present on the surface of affected foley catheters.
|
FDA
Z-2226-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 23, 2026
|
Details |
|
OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small, 13 Degree 10mm X 6mm, 010-113-1006-2/Small, 13 Degree, 10mm X 6mm - Oblique, 010-113-1208/Small 13 Degree 12mm X 8mm, 010-113-1410/Small 13 Degree 14mm X 10mm, 010-113-1612/Small 13 Degree 16mm X 12mm, 010-119-1407/19 Degree 14mm X 7mm, 010-119-1609/Small 19 Degree 16mm X 9mm, 010-119-1811/Small 19 Degree 18mm X 11mm, 010-1
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and/or the need to select an alternative implant.
|
FDA
Z-2213-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 23, 2026
|
Details |
|
Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 722229. 2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230. 3. Azurion 5 M12; Model Numbers: 722227, 722231. 4. Azurion 5 M20; Model Numbers: 722228, 722232, 722281. 5. Azurion 7 B12; Model Numbers: 722067, 722225, 722235. 6. Azurion 7 B20; Model Numbers: 722068, 722226, 722236. 7. Azurion 7 M12; Model Numbers: 722078, 722223, 722233. 8. Azurion 7 M20; Model Numbers: 722079, 722224, 722234, 7
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.
|
FDA
Z-2225-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 28, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2221-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2217-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Swan-Ganz Pacing Catheter, Models: D200F7;
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
|
FDA
Z-2204-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 8, 2026
|
Details |
|
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2214-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2216-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2219-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2218-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
|
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
|
FDA
Z-2227-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 28, 2026
|
Details |
|
Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
|
FDA
Z-2203-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 8, 2026
|
Details |
|
Improperly Tightened Shock Bolts
Ember Recreational Vehicles, INC. (Ember) is recalling certain 2026-2027 Touring Edition recreational trailers, equipped with certain Curt Touring Coil Suspensions. The shock bolts may have been incorrectly tightened. Broken shock retainer bolt heads and washers may detach and become a road hazard, increasing the risk of a crash.
|
NHTSA
26V339000
|
Vehicle | High |
May 27, 2026
Recall: May 27, 2026
|
Details |
|
Do Not Drive: Loss of Control from Control Arm Separation
Ford Motor Company (Ford) is recalling certain 2021-2026 Bronco Sport and 2022-2026 Maverick vehicles. The front lower control arm ball joints may have been incorrectly installed or incorrectly repaired at the vehicle assembly plant, allowing the control arm to disconnect from the front wheel knuckle. A detached control arm can cause a loss of vehicle control, increasing the risk of a crash.
|
NHTSA
26V340000
|
Vehicle | Critical |
May 27, 2026
Recall: May 27, 2026
|
Details |
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
Use the source notes to understand which agency published the notice and what type of product it covers.
Latest Consumer Product Recalls
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
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.
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.
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
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
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.