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 26 - 50 of 3,083 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
|
FDA
H-1146-2026
|
Food | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
EC Hot Links Seasoning 45.05#
Undeclared Sesame allergen
|
FDA
H-1140-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
FDA
H-1143-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details | |
|
Smoked Sausage Spice 32.86#
Undeclared Sesame allergen
|
FDA
H-1138-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.
|
FDA
Z-2714-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 5, 2026
|
Details |
|
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2696-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
|
FDA
Z-2701-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Feb 16, 2026
|
Details |
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Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
|
FDA
Z-2700-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Feb 16, 2026
|
Details |
|
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2697-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU, INTRACEPT ACCESS INSTRUMENTS 2 VB/RLV0065, INTRACEPT ACCESS INSTRMNTS ADDITIONAL VB/RLV0075, INTRACEPT ACCESS INSTRMNTS ADDTL VB EU/RLV0075-EU
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.
|
FDA
Z-2694-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 22, 2026
|
Details |
|
VITEK 2 AST-N447 TEST KIT Product reference 424620
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
|
FDA
Z-2715-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 4, 2026
|
Details |
|
TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
|
FDA
Z-2716-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 8, 2026
|
Details |
|
Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
|
FDA
Z-2712-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
|
Details |
|
Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed for interstitial brachytherapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
|
FDA
Z-2711-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
|
Details |
|
5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF Standard Blood Tubing Set; Model Number: 03-5300-3. 4. 5008X HD/HDF With CLiC Blood Tubing Set; Model Number: 03-5300-3C. 5. 5008X HD/HDF With Twister Blood Tubing Set; Model Number: 03-5350-8.
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.
|
FDA
Z-2702-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 11, 2026
|
Details |
|
Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
|
FDA
Z-2710-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
|
Details |
|
Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.
The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patient results.
|
FDA
Z-2703-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 8, 2026
|
Details |
|
Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2695-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system designed for surgeons to perform minimally invasive surgery.
Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.
|
FDA
Z-2717-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 9, 2026
|
Details |
|
Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flexible/rigid
Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.
|
FDA
Z-2676-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 5, 2026
|
Details |
|
MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).
|
FDA
Z-2698-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 27, 2026
|
Details |
|
KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,
A product error defect may cause incorrect bracket placement.
|
FDA
Z-2699-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 8, 2026
|
Details |
|
GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.
Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.
|
FDA
Z-2713-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 18, 2026
|
Details |
|
Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Surgical dressing manufactured out of specification (greater thickness).
|
FDA
Z-2677-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 8, 2026
|
Details |
|
Incorrect GAWR on Certification Label/FMVSS 110
Nissan North America, Inc. (Nissan) is recalling certain 2020-2026 Nissan Armada, 2011-2013 Infiniti QX56, and 2014-2027 QX80 vehicles equipped with 22" wheels. The Gross Axle Weight Rating (GAWR) listed on the certification label is incorrect, which can allow the vehicle to be overloaded. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." An overloaded vehicle can increase the risk of a crash.
|
NHTSA
26V455000
|
Vehicle | High |
Jul 15, 2026
Recall: Jul 15, 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.