Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

301–325 of 6113

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 & Parmesa
Category
Food
Distribution
10 states
SevereFDA (Food)·H-0616-2026·2026-04-01
Slow Roasted Diced Tomatoes Recalled for Possible Metal Fragments
Sevillo Fine Foods is recalling Slow Roasted Diced Tomatoes (24 lb bulk packages, UPC 00823338008216) because the product may contain metal fragments.
Product
Slow Roasted Diced Tomatoes (SKU 821, UPC 00823338008216). Frozen. Shelf life: 365 days (frozen) from date of manufacture; 30 days (refrigerated, unopened); 7 days (refrigerated, opened). Plastic poly liner inside cardboard box (bulk). Net weight: 24 lbs. Firm: Sevillo Fine Foods
Category
Food
Distribution
2 states
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. Produ
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0591-2026·2026-04-01
Trader Joe's Japanese Style Fried Rice recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.
Product
Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb. per bag. Retail bag UPC 00979085. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per ca
Category
Food
Distribution
43 states
SevereFDA (Food)·H-0593-2026·2026-04-01
Ajinomoto Teppanyaki Style Vegetable Fried Rice recalled for glass fragments
Ajinomoto Foods North America is recalling Teppanyaki Style Vegetable Fried Rice due to the presence of glass fragments ranging from 1–3 cm long. Consumers should not eat affected products and should discard or return them.
Product
Item 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice - Japanese-style fried rice made with colorful vegetables in an aromatic garlic butter sauce. There are 6/9oz. bags per box or 54oz per box. Retail box UPC 071757508835. Product packaging is flexible bags in a master c
Category
Food
Distribution
43 states
SevereFDA (Devices)·Z-1577-2026·2026-04-01
16F Splittable Sheath Introducer Recalled Due to Splitting Defect
Merit Medical's 16F sheath introducers may fail to split properly, posing risks of hemorrhage, foreign body retention, and blood clots during vascular procedures. Approximately 368,264 units distributed worldwide are affected.
Product
16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1578-2026·2026-04-01
DuraMax Chronic Hemodialysis Catheter recalled for design defect that prevents proper splitting
Merit Medical Systems is recalling the DuraMax Chronic Hemodialysis Catheter due to a design defect that prevents proper splitting, potentially causing hemorrhage, blood clots, device malfunction, and complications during dialysis treatment.
Product
DuraMax Chronic Hemodialysis Catheter, REF: H787103028015/A, H787103028025/A, H787103028031/A, H787103028035/A, H787103028041/A, H787103028045/A, H787103028051/A, H787103028055/A, H787103028061/A, H787103028075/A, H787103028085/A, H787103028095/A, H787103028165/A, H787103028181/A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1567-2026·2026-04-01
Flexible Cryoprobes May Rupture During Surgical Activation
Erbe USA Inc recalls 8,284 flexible cryoprobes used in surgical procedures. The devices may rupture or burst during activation, posing a risk to patient safety.
Product
Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1614-2026·2026-04-01
Philips Respironics Trilogy Evo Ventilator May Deliver Incorrect Tidal Volume
Philips Respironics Trilogy Evo ventilators may deliver incorrect tidal volume to patients when used with non-pneumatic nebulizers. This discrepancy between set and delivered volume poses a risk to home-use patients.
Product
Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1566-2026·2026-04-01
Flexible Cryoprobe Surgical Instruments Recalled for Potential Rupture During Use
Erbe USA Inc is recalling 64,216 Flexible Cryoprobes used in surgery because they may rupture or burst during activation. Affected units were distributed nationwide.
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-1617-2026·2026-04-01
Philips Respironics Trilogy Evo Ventilator Tidal Volume Discrepancy Recall
Philips Respironics Trilogy Evo Universal ventilators may have tidal volume discrepancies when used with non-pneumatic nebulizers. Approximately 113,717 units distributed worldwide are affected by this Class I recall.
Product
Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1576-2026·2026-04-01
ProGuide Chronic Dialysis Catheters Recalled for Design Defect Risk
Merit Medical Systems is recalling ProGuide Chronic Dialysis Catheters due to a design defect in the sheath introducer that may not split properly. This could lead to hemorrhage, blood clots, or loss of vascular access.
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 (Devices)·Z-1615-2026·2026-04-01
Philips Trilogy Evo O2 Ventilator Breathing Support Discrepancy with Non-Pneumatic Nebulizers
Philips Respironics Trilogy Evo O2 ventilators may not deliver the correct breathing support when used with non-pneumatic nebulizers. Verify nebulizer compatibility and contact Philips for guidance.
Product
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1588-2026·2026-04-01
Handy Solutions Neck and Shoulders Heating Pad may overheat and burn
Handy Solutions Neck & Shoulders Heating Pad (Model 25607) recalled nationwide. Device may overheat if folded or placed under body, causing burning smell, material damage, and potential burns to users.
Product
Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·26339·2026-03-26
Nexgrill metal wire grill brushes recalled for bristle ingestion and injury hazard
Nexgrill is recalling 10.2 million metal wire grill brushes because bristles can detach and be ingested, posing a risk of serious internal injury. Five consumers have swallowed bristles and sought medical treatment.
Product
Metal Wire Bristle Grill Brushes
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·H-0581-2026·2026-03-25
Great Value Fat Free Cottage Cheese Recalled for Potential Under-Pasteurization
Saputo Cheese USA is recalling Great Value Fat Free Cottage Cheese Small Curd due to potential under-pasteurization caused by a broken seal on the pasteurizer. The product was distributed to multiple states.
Product
Great Value Fat Free Cottage Cheese Small Curd 0% Milkfat NET WT 24OZ UPC 0 78742 37339 3 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
Category
Food
Distribution
11 states
SevereFDA (Food)·H-0576-2026·2026-03-25
MID EAST Jordanian Zaatar spice mix recalled for undeclared allergens
Kradjian Importing Company is recalling MID EAST Jordanian Zaatar spice mix because it contains undeclared sesame and wheat, which are major allergens.
Product
MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack Inc. Sunvalley, CA 91354
Category
Food
Distribution
0 states
SevereFDA (Food)·H-0573-2026·2026-03-25
Butter Powder Recalled Due to Positive Salmonella Contamination
Bluegrass Ingredients Inc. is recalling Butter Powder (50 LB bags, Product Number BDF0006, Lot 6018) due to positive Salmonella contamination. The product was distributed to Florida, Illinois, and Maryland.
Product
Butter Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Category
Food
Distribution
3 states
SevereFDA (Food)·H-0572-2026·2026-03-25
Butter-Rich Powder Recalled Due to Potential Salmonella Contamination
Bluegrass Ingredients Inc. is recalling Butter-Rich Powder (50 LB. bags) due to potential Salmonella contamination. The product was distributed to Florida, Illinois, and Maryland.
Product
Butter-Rich Powder, Net Weight 50 LB., packaged in a multiply Kraft bag with poly liner
Category
Food
Distribution
3 states
SevereFDA (Food)·H-0583-2026·2026-03-25
Great Value Cottage Cheese Small Curd Recall Due to Potential Underpasteurization
Saputo Cheese USA is recalling Great Value Cottage Cheese products because a broken pasteurizer seal may have resulted in underpasteurized product. The recall affects 16oz, 24oz, and 3lb containers distributed to multiple states.
Product
Great Value Cottage Cheese Small Curd 4% Milkfat NET WT 16oZ UPC 0 78742 37235 8; 24oz UPC 0 78742 37236 5 & 3lb UPC 0 78742 14797 0 DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
Category
Food
Distribution
11 states
SevereFDA (Food)·N/A·2026-03-25
White Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
Shaman Botanicals, LLC is recalling White Vein Advanced Alkaloids Chewable Tablets because testing found the active ingredient 7-hydroxymitragynine is present in a quantity greater than the labeled specification.
Product
Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 3
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0528-2026·2026-03-25
Webcol Alcohol Prep Pads Recalled Due to Microbial Contamination
Cardinal Health is recalling approximately 174.3 million boxes of Webcol Alcohol Prep pads nationwide due to non-sterile conditions caused by microbial contamination. The contaminated products should not be used.
Product
Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·26333·2026-03-19
Frigidaire Gas Ranges Recalled for Delayed Ignition Burn Hazard
Electrolux is recalling about 174,800 Frigidaire gas ranges for a delayed oven ignition hazard that has caused 30 reported burn injuries. Free repairs are available.
Product
Frigidaire Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26328·2026-03-19
Wagner 900 Series Power Steamers Recalled Due to Burn Hazard
Wagner Spray Tech recalled about 700,000 power steamers because the hose and nozzle can get excessively hot, causing burns. Over 50 consumers reported burn injuries, many first- or second-degree.
Product
Wagner 900 Series Power Steamers
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Food)·H-0564-2026·2026-03-18
Made Fresh Salads Sundried Tomato Cream Cheese Recalled for Listeria Contamination
Made Fresh Salads brand Sundried Tomato Cream Cheese (5 lb tubs) is being recalled because it may be contaminated with Listeria monocytogenes. Consumers should not eat the product and should contact the manufacturer or their retailer.
Product
Made Fresh Salads brand Sundried Tomato Cream Cheese; 5 lb white plastic tub
Category
Food
Distribution
0 states