Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1651–1675 of 26155

HighFDA (Devices)·Z-1489-2026·2026-03-11
Olympus Single Use Biopsy Valve Recalled Due to Rubber Fragment Detachment Risk
Olympus is recalling its Single Use Biopsy Valve (Model MAJ-1218) due to potential rubber fragments detaching during use. The product has been distributed nationwide.
Product
Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0354-2026·2026-03-11
Metoprolol succinate tablets recalled for failed dissolution specifications
Teva Pharmaceuticals is recalling 18,780 bottles of metoprolol succinate extended-release tablets nationwide due to failed dissolution specifications that may reduce medication effectiveness.
Product
METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0372-2026·2026-03-11
Hand sanitizing wipes recalled due to manufacturing practice deviations
ACME UNITED CORPORATION is recalling WP WipesPlus Hand Sanitizing Wipes nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The company voluntarily initiated the recall following FDA notification.
Product
WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67151-727-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1488-2026·2026-03-11
Olympus Biopsy Valve Recalled Due to Potential Rubber Fragment Detachment
Olympus Corporation is recalling approximately 95,882 boxes of MAJ-210 Single use Biopsy Valves nationwide due to potential for rubber fragments to detach during endoscopic procedures.
Product
Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1475-2026·2026-03-11
GE Healthcare Centricity Universal Viewer: Patient Information May Not Match Images
GE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client software versions ZFP v6.0 SP11.6, SP11.6.0.1, and SP11.6.1 due to a data integrity issue where patient information may not match displayed images on systems with Patient Timeline installed.
Product
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1490-2026·2026-03-11
Esaote Endocavity Ultrasonic Probe Recalled for Potential Liquid Leak
Esaote is recalling Endocavity ultrasonic probes (Model E 3-12) due to a potential weakness that may cause liquid leakage from the cable terminal area. Five units distributed in North Carolina and Texas are affected.
Product
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2026·2026-03-11
Toric Implantable Collamer Lens Recall: Mislabeled Length May Cause Angle Closure
Staar Surgical is recalling 7 EVO+ Visian Toric Collamer Lenses (Model VTICM5) that were labeled as 12.1 mm but are actually 12.6 mm. The oversized lenses may cause excessive vault, leading to angle closure and elevated intraocular pressure requiring lens exchange.
Product
EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1485-2026·2026-03-11
Aesculap MINOP Trocar Recalled for Potential Shaft Length Defect
Aesculap Inc. is recalling 126 units of its MINOP TROCAR 150MM surgical instrument (Model FF399R) because the trocar shaft may be longer than specification. The affected units were distributed to healthcare facilities nationwide.
Product
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1491-2026·2026-03-11
Medical Device Recall: Free Protein S Test Kit Results May Be Inaccurate
Diagnostica Stago is recalling STA Liatest Free Protein S diagnostic kits that may produce inaccurate test results, underestimating free protein S levels in patient plasma samples.
Product
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use on STA-R¿ and STA Compact¿ for the quantitative antigenic assay of free protein S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2026·2026-03-11
B. Braun Infusion Needle Recall: Potential Dull or Broken Needle Tip
B. Braun is recalling 21,000 units of its 21GA WINGED INFUSION needle due to the potential for needle tips to be dull, blunt, or break during use. The defect affects subcutaneous implant procedures.
Product
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneou
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2026·2026-03-11
Olympus ShockPulse-SE Lithotripsy System Generator Connector Malfunction Recall
Olympus is recalling 602 ShockPulse-SE Lithotripsy Systems due to generator malfunction caused by connector damage. The generator may fail to recognize the transducer, preventing proper device operation during stone fragmentation procedures.
Product
Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0540-2026·2026-03-11
VERGANI 1944 MILANO Pandoro Classico Gluten Free Cake Recall
Italianway Import, Inc. is recalling VERGANI 1944 MILANO Pandoro Classico Gluten Free cake due to potential contamination with Teflon fragments from flaking cooking molds.
Product
VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free, 600g NET WT. 1 LBS. 5.2 OZ., packaged in paper cartons, 6 units per case. Lot 217666, UPC 8002114019833
Category
Food
Distribution
3 states
HighFDA (Food)·H-0543-2026·2026-03-11
Junebar Chocolate Cherry Snack Bars Recalled for Undeclared Milk and Soy
Juniper Granola, LLC is recalling Junebar Chocolate Cherry All Natural Snack Bars because they contain undeclared milk and soy, posing a risk to consumers with allergies to these ingredients.
Product
Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN CHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), DRIED CHERRIE
Category
Food
Distribution
0 states
HighFDA (Food)·H-0544-2026·2026-03-11
Tippy Toes Baby Food Recalled for Potential Patulin Contamination
Tippy Toes apple pear banana baby food (6 months & up) is being recalled due to potential contamination with patulin. Consumers who have purchased this product should not feed it to infants.
Product
tippy toes apple pear banana 6 months & up baby food 2-4OZ (113g) PACKS NET WT 8 OZ (226g) DISTRIBUTED BY TOPCO ASSOCIATES LLC ELK GROVE VILLAGE, IL 60007 1-888-423-0139 PRODUCT OF USA UPC: 036800265783
Category
Food
Distribution
1 state
HighFDA (Food)·H-0542-2026·2026-03-11
Junebar Peanut Chocolate Chip Snack Bars Recalled for Undeclared Milk and Soy
Juniper Granola is recalling Junebar Peanut Chocolate Chip All Natural Snack Bars because they contain undeclared milk and soy, which pose a risk to consumers with allergies to these ingredients.
Product
Junebar Peanut Chocolate Chip All Natural Snack Bar; INGREDIENTS: ORGANIC PEANUT BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN SHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), PEANUTS,
Category
Food
Distribution
0 states
HighFDA (Food)·H-0574-2026·2026-03-11
Karns Foods Mini Dark Chocolate Raspberry Cups recalled for undeclared peanuts
Karns Prime And Fancy Foods is recalling Mini Dark Chocolate Raspberry Cups because they may contain undeclared peanuts. The product was distributed only in Pennsylvania.
Product
Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakout
Category
Food
Distribution
0 states
HighNHTSA·24V900000·2026-03-11
Honda Passport fuel filler separation fire hazard recall
Honda is recalling certain 2024 Passport and related models due to fuel filler neck and pipe separation that could allow fuel leakage and increase fire risk. Dealers will inspect and repair affected vehicles at no charge.
Product
HONDA — 2024 HONDA PASSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0384-2026·2026-03-11
FDA recalls Temozolomide 5mg capsules for quality failures
Rising Pharma is recalling 1,200 bottles of Temozolomide 5mg capsules (lot 1TM0524003A) nationwide due to out-of-specification impurities and degradation detected during stability testing.
Product
TEMOZOLOMIDE — TEMOZOLOMIDE (TEMOZOLOMIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0393-2026·2026-03-11
Semaglutide Injectable Vial Recalled Due to Lack of Sterility Assurance
Semaglutide injectable vials (lot 240903) are being recalled due to lack of sterility assurance. The product was distributed in Ohio with expiration 9/30/2026.
Product
Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-06
Category
Drug
Distribution
1 state
HighFDA (Drugs)·D-0385-2026·2026-03-11
Vasocaine Spray Recalled Due to Unsupported Expiration Dates
HTO Nevada Inc. is recalling FIVE-STAR VASOCAINE Spray because stability data does not support the stated expiration dates on 27,380 bottles distributed nationwide.
Product
FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0394-2026·2026-03-11
Tirzepatide 10mg Injectable Vials Recalled for Sterility Assurance Issues
New Life Pharma LLC is recalling 23 vials of Tirzepatide 10mg injectable due to lack of assurance of sterility. The affected batch (Lot 240709) was distributed in Ohio.
Product
Tirzepatide Inj, 10mg, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-03.
Category
Drug
Distribution
1 state
HighFDA (Drugs)·D-0363-2026·2026-03-11
Max Packaging Antibacterial Towelettes Recalled for Manufacturing Deviations
ACME United Corporation is recalling Max Packaging Antibacterial Towelettes (NDC 59647-750-01) due to manufacturing practice deviations. Specific lot numbers are affected nationwide.
Product
Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0379-2026·2026-03-11
Semaglutide Compounding Powder Recalled for Failed Process Validation
Harbin Jixianglong Biotech's semaglutide compounding powder is recalled nationwide for failing to complete process validation and bacterial endotoxin testing before distribution. No illnesses have been reported.
Product
Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04 Manufacturer: Harbin Jixianglong Biotech Co., Ltd., North of Baoan Road, East of Changqing Street,
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V699000·2026-03-10
2024-2026 Tesla Cybertruck Front Parking Lights Brightness Recall
Tesla is recalling 2024-2026 Cybertruck vehicles due to front parking lights that exceed maximum brightness limits. The overly bright lights can reduce visibility for oncoming drivers, increasing the risk of crashes.
Product
TESLA — 2024 TESLA CYBERTRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V723000·2026-03-09
2024 Volkswagen Atlas and Atlas Cross Sport brake master cylinder defect
Volkswagen is recalling 1,591 model year 2024 Atlas and Atlas Cross Sport vehicles due to an incorrectly assembled brake master cylinder that can block brake fluid, causing brake failure. Owners should contact Volkswagen for a free replacement.
Product
VOLKSWAGEN — 2024 VOLKSWAGEN ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide

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1651–1675 of 26155