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.
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.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
|
FDA
Z-2559-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Apr 30, 2026
|
Details |
|
Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.
|
FDA
Z-2526-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Apr 21, 2026
|
Details |
|
Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM SET UP
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
|
FDA
Z-2452-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 6, 2026
|
Details |
|
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO DRAPE PACK (ADLUG)642-LF DYNJ47665D ANGIO PACK DYNJ30565D ANGIOGRAPHY PACK-LF DYNJ0854485V ARTERIOGRAM DYNJ28082D DYNJ28082F CARDIAC CATH DYNJ67349 CARDIAC CATH PACK DYNJ57874C CATH I PLUS-LF DYNJSCL100 CATH III PLUS-LF DYNJSCL300 CATH LAB ANGIOGRAPHY PACK DYNJ50779F CATH LAB PACK DYNJ41088B DYNJ48085 CATH LAB TRAY DYNJ37389N DYNJ37389O CATH PACK DYNJ62595A DYNJ69997 EP DRAPE PACK-LF DYNJ47645B HOSPITAL REGIONAL DE CONCEPCIO DYNJ67918A INTERVENTIONAL PACK DYNJ56666C INTERVENTIONAL RAD PACK DYNJ44100L INTERVEN
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
|
FDA
Z-2592-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Feb 27, 2026
|
Details |
|
Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
|
FDA
Z-2557-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Apr 30, 2026
|
Details |
|
Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product Code: 1000434.
Potential for thrombus formation during prolonged use of the introducer.
|
FDA
Z-2599-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 22, 2026
|
Details |
|
Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Size 9, 9+ 10mm Thicknes Component: N/A
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
|
FDA
Z-2578-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 11, 2026
|
Details |
|
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Software anomaly that causes a false display of error code 5018.
|
FDA
Z-2554-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 5, 2026
|
Details |
|
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
|
FDA
Z-2580-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 11, 2026
|
Details |
|
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO CATH COMBINED PACK DYNJ43609S ANGIO PACK DYNJ67987D DYNJ80317A ANGIO SPECIAL PROCEDURE-LF DYNJ38412C ANGIOGRAM SET UP PACK DYNJ66260A ANGIOGRAPHY PACK DYNJ44293I ANGIOGRAPHY PACK-LF DYNJ0854485W CARDIAC CATH PACK DYNJ82709 CARDIAC CATH PACK-LF DYNJ0261554AL DYNJ31103F CATH LAB ANGIO TRAY DYNJ83506 CATH LAB PACK DYNJ66366C MSC-GREEN BAY ST VINCENT SAMPC0686 NEUROLOGICAL CATH PACK DYNJ63434B OR HYBRID-MRMC DYNJ907758B STEWARD OR ANGIO PACK GSS DYNJ80925B
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
|
FDA
Z-2582-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Feb 27, 2026
|
Details |
|
8/9.5oz Tub Nut - Sunflower Seed
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
|
FDA
H-1120-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 29, 2026
|
Details |
|
5# Sunflower Seeds C/S
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
|
FDA
H-1121-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 29, 2026
|
Details |
|
Joy Orange Lassi 16 oz.
Product not adequately pasteurized
|
FDA
H-1093-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 23, 2026
|
Details |
|
FDA
H-1106-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
FDA
H-1124-2026
|
Food | High |
Jul 1, 2026
Recall: May 13, 2026
|
Details | |
|
FDA
H-1096-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.
Potential presence of Salmonella.
|
FDA
H-1116-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 28, 2026
|
Details |
|
FDA
H-1105-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
FDA
H-1098-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in transparent, flexible plastic wrap. (20 bonbon pieces per 400g box). UPC 5304000050757
Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
|
FDA
H-1110-2026
|
Food | High |
Jul 1, 2026
Recall: May 21, 2026
|
Details |
|
Joy Strawberry Lassi 16 oz.
Product not adequately pasteurized
|
FDA
H-1086-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 23, 2026
|
Details |
|
FDA
H-1097-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
Joy Mango Lassi 16 oz., 64 oz.
Product not adequately pasteurized
|
FDA
H-1081-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 23, 2026
|
Details |
|
FDA
H-1099-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
FDA
H-1104-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details |
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 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 notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
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.
Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
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.
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
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.
Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.