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 the agency’s own highest classification or reported deaths or serious injuries, 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

4301–4325 of 114837

SevereFDA (Food)·H-0619-2026·2026-04-01
Focaccia Bread Products Recalled for Metal Fragments
Bakkavor is recalling roasted tomato and parmesan focaccia bread sold under multiple retail brands due to metal fragments discovered in the products. The metal originated from roasted tomatoes supplied by an ingredient supplier.
Product
Roasted Tomato Parmesan Focaccia Bread sold under the brand names of FREDERIK'S by meijer SLOW-ROASTED TOMATO & SHREDDED PARMESAN CHEESE NET WT 13.75 OZ (390g) UPC 7 13733 88387 0 DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544; fresh & simple Roasted Tomato &…
Category
Food
Distribution
10 states
SevereFDA (Devices)·Z-1576-2026·2026-04-01
ProGuide chronic dialysis catheters recalled as Class I over sheath introducer defect
Merit Medical is recalling ProGuide Chronic Dialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Product
ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0649-2026·2026-04-01
Doraditas de Azucar recalled due to missing allergen labeling
Distribuidora de Alimentos Sendero LLC is recalling Doraditas de Azucar because the product label is missing declarations for wheat and soy allergens.
Product
Doraditas de Azucar UPC 5901234123457
Category
Food
Distribution
1 state
SevereFDA (Food)·H-0630-2026·2026-04-01
Lucerne 2% Cottage Cheese recalled for metal fragments
Lucerne 2% Cottage Cheese 24 oz. tubs are being recalled due to the potential presence of metal spring fragments. Consumers who have purchased affected product should not consume it.
Product
Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz. Perishable and keep refrigerated. Consumer package is a plastic cup with foil lid and clear plastic lid. UPC 0 21130 07662 8. Distributed by Lucerne Foods, Inc PO Box 99, Pleasanton, CA.…
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-1567-2026·2026-04-01
Erbe flexible cryoprobe 20402-410 recalled as Class I over rupture
Erbe USA is recalling the Flexible Cryoprobe REF 20402-410 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Product
Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1566-2026·2026-04-01
Erbe flexible cryoprobe 20402-401 recalled as Class I over rupture
Erbe USA is recalling the Flexible Cryoprobe REF 20402-401 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Product
Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1615-2026·2026-04-01
Trilogy Evo O2 ventilator recalled as Class I over tidal volume
Philips Respironics is recalling the Trilogy Evo O2 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Product
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0632-2026·2026-04-01
Nuts.com Espresso Malted Milk Balls Recalled for Undeclared Wheat and Soy
Nuts.com is recalling Espresso Malted Milk Balls sold in 1 lb. and 20 lb. packages because the labels do not declare wheat and soy allergens that are present in the product.
Product
Nuts.com, Espresso Malted Milk Balls, 1 lb. sealed pouch & 20 lb. clear poly bag in Nuts.com cardboard box . Packages are only sold individually .
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1579-2026·2026-04-01
BioFlo DuraMax catheters recalled as Class I over sheath introducer defect
Merit Medical is recalling BioFlo DuraMax Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Product
BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H965103028031/EU, H965103028041/A, H965103028041/EU, H965103028051/A, H965103028051/EU, H965103028061/A, H965103028061/EU, H965103028070/A, H965103028070/EU, H965103028080/A…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V210000·2026-04-01
Isuzu and Chevrolet Commercial Trucks Recalled for Wire Harness Chafing
Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.
Product
ISUZU — ISUZU CHEVROLET LCF 4500HD, NPR HD, CHEVROLET LCF 5500XD, NPR XD
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1568-2026·2026-04-01
Erbe flexible cryoprobe 20402-411 recalled as Class I over rupture
Erbe USA is recalling the Flexible Cryoprobe REF 20402-411 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Product
Flexible Cryoprobe (OD 2.4mm, L1.15mm) REF: 20402-411. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1588-2026·2026-04-01
Heating pad recalled as Class I because folding causes excessive temperatures
Navajo Manufacturing is recalling the Handy Solutions Neck & Shoulders Heating Pad because folding it during use raises power density in the folded area, causing excessive temperatures the limit device cannot sense.
Product
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1640-2026·2026-04-01
Olympus PK cutting forceps jaws may break from defective welds
Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1607-2026·2026-04-01
I.T.S. hand locking plates heat more in MRI than instructions state
I.T.S. GmbH is recalling the HLS Hand Locking Plates System because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.
Product
HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers. 1. Cortical Screw; Article Numbers: 32151-6, 32151-8, 32151-9, 32151-10, 32151-11, 32151-12, 32151-13, 32151-14, 32151-15, 32151-16, 32151-18, 32151-20. 2. HLS Plate, 2…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1644-2026·2026-04-01
Olympus PKS cutting forceps jaws may break from defective welds
Olympus is recalling PKS Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Product
Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0590-2026·2026-04-01
Chilli Spanish Peanuts Recalled for Glass Contamination Risk
Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bags, Lot #260230) due to glass fragments found in sealed containers.
Product
Chilli Spanish Peanuts, Treasured Harvest brand, 25lb clear plastic bag container. UPC:none Item code: 2608-25
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0602-2026·2026-04-01
Bulk Colustrum Powder Missing Milk Allergen Declaration
Herbal Creations USA is recalling bulk packaged Colustrum Powder because the product label does not declare milk as an allergen ingredient, posing a risk to consumers with milk allergies.
Product
Bulk packaged Colustrum Powder. packaged with generic product label.
Category
Food
Distribution
0 states
HighFDA (Food)·H-0623-2026·2026-04-01
Pan de Bono Cheese Bread Recalled for Undeclared Soy Allergen
South Florida Food, LLC is recalling Pan de Bono (Cheese Bread) because the product contains undeclared soy, a common allergen that poses a health risk to consumers with soy allergies.
Product
Pan de Bono (Cheese Bread), 100 units per Paper Cardboard Box, Net Wt 14.4 lb. KEEP FROZEN
Category
Food
Distribution
1 state
HighNHTSA·26V207000·2026-04-01
Mack Recalls 2025-2027 Trailers Due to Turn Signal Software Defect
Mack Trucks is recalling 2025-2027 Pioneer and 2027 Anthem trailers because turn signals may not function properly, increasing crash risk.
Product
MACK — MACK ANTHEM AN (4), PIONEER PR (4)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2026·2026-04-01
GE Imactis CT navigation may show needle trajectory that differs from actual
GE Medical Systems is recalling the Imactis CT-Navigation System because of a potential discordance between the simulated needle trajectory and tip position and the actual trajectory and tip position.
Product
Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0615-2026·2026-04-01
Savannah Bee Company Honey BBQ Sauce Mustard Undeclared Allergens
Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.
Product
SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES. INGREDIENTS: MUSTARD (DISTILLED VINEGAR, WATER, MUSTARD SEED, SALT, SPICES (INCLUDING PAPRIKA AND TUMERIC), NATURAL FLAVOR, GARLIC), HONEY, WATER, DISTILLED VINEGAR, SUGAR, TOMATO CONCENTRATE…
Category
Food
Distribution
45 states
HighFDA (Devices)·Z-1604-2026·2026-04-01
I.T.S. distal ulna plates heat more in MRI than instructions state
I.T.S. GmbH is recalling the Distal Ulna Locking and Ulna Osteotomy Locking Systems because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and corresponding article numbers. 1. I.T.S. DUL (Distal Ulna Locking) System, Distal Ulna Plate; Article Numbers: 21232-3, 21232-4, 21232-6, 21233-3, 21233-4, 21233-6…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0594-2026·2026-04-01
Ajinomoto Japanese-Style Vegetable Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America Inc. is recalling Item 5650893 Japanese-Style Vegetable Fried Rice because some packages may contain glass fragments measuring 1–3 cm long and 2–4 mm wide.
Product
Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed, fried tofu, edamame, and other colorful vegetables in an umami dashi sauce Net wt. 17oz. Retail box UPC 071757508934. Product packaging is flexible bags in a master case or flexible bags in…
Category
Food
Distribution
43 states
HighFDA (Devices)·Z-1598-2026·2026-04-01
I.T.S. straight and forearm plates heat more in MRI than stated
I.T.S. GmbH is recalling Straight Plates with Angular Stability, including forearm and compression plates, because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.
Product
I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article numbers. 1. Forearm Plate, Curved; Article Numbers: 21604-6, 21604-9. 2. Forearm Plate, Straight; Article Numbers: 21605-11, 21605-6, 21605-9. 3. Straight Compression…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1609-2026·2026-04-01
Beckman Coulter MicroScan gram-negative panels may contain contaminated wells
Beckman Coulter is recalling one lot of MicroScan Neg MIC 56 panels due to the likely presence of contamination in one or more wells.
Product
MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.
Category
Medical Device
Distribution
Distributed nationwide

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4301–4325 of 114837