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

1176–1200 of 5642

SevereFDA (Devices)·Z-1814-2024·2024-05-29
BiPAP A30 Ventilator Recall: Risk of Therapy Interruption and Respiratory Failure
Philips Respironics BiPAP A30 Ventilators may experience interruption or loss of therapy during a Ventilator Inoperative alarm, potentially causing severe respiratory compromise or death in vulnerable patients.
Product
BiPAP A30 Ventilator, Part Number 1111143 (US and OUS) OUS Only: Part Numbers 1111144 1111145 1111147 1111148 1111149 1111150 1111154 1111181 1116155 1111144L 1111144M 1111144V BR1111143 CN1111143 R1111143 R1111150 R1111181
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1262-2024·2024-05-29
Fresh soft white cheese recalled for potential Listeria contamination
Tama Corporation is recalling Queso de mano (fresh soft white cheese) due to potential Listeria monocytogenes contamination. The affected product was distributed in Utah.
Product
Queso de mano, Fresh soft white cheese, NET WT 24 oz.(640g), Keep Refrigerated, plastic container, packed 12 plastic containers of 24 oz per case
Category
Food
Distribution
1 state
SevereFDA (Food)·F-1252-2024·2024-05-29
Geissler's Supermarket Pink Lady Salmon Roll Recalled for Undeclared Egg Allergen
Geissler's Supermarket is recalling Pink Lady Salmon & Avo Roll Combo sushi due to undeclared egg allergen. Consumers with egg allergies risk allergic reactions if they consume this product.
Product
Geissler's Supermarket Pink Lady Salmon &Avo Roll Combo (sushi roll) Ingredients read in part: "***INGREDIENTS: SALMON, AVOCADO, WATER. NORI.WHITESTEAMEORICE. VINEGAR. SUGAR. SALT.LEMON.MIRIN. WASABI. GINGER. SOYSAUCE (WHEAT, SOYBEANS,ALCOHOL) HOT SAUCE: SUGAR. MAYO. CHILI, SRIR
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1256-2024·2024-05-29
Geissler's Supermarket Shrimp Tempura and Lobster Roll Recalled for Undeclared Wheat
Geissler's Supermarket is recalling Shrimp Tempura and Lobster Roll products sold in Connecticut and Massachusetts because they contain undeclared wheat, a common allergen.
Product
Geissler's Supermarket Shrimp Tempura and Lobster Roll 12 oz.
Category
Food
Distribution
2 states
SevereFDA (Food)·F-1247-2024·2024-05-29
Sammy's Milk Goat Formula Recalled for Misleading Infant Safety Claims
Sammy's Milk goat formula is recalled for marketing it as safe for infants. The unapproved product does not comply with FDA infant formula manufacturing requirements.
Product
Sammy's Milk GOAT MILK TODDLER FORMULA, 25.68 oz (78g) pouch
Category
Food
Distribution
43 states
SevereFDA (Devices)·Z-1817-2024·2024-05-29
Philips OmniLab Advanced + Ventilator May Experience Unexpected Therapy Loss
Philips OmniLab Advanced + Ventilators may experience an alarm condition that interrupts or stops therapy delivery. This interruption may lead to inadequate breathing support, low oxygen levels, and potentially fatal respiratory failure.
Product
OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 1111126 1111127 1111138 1111141 1111142 KR1111127 R1111122 R1111123 R1111124 U1111122 U1111124
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1813-2024·2024-05-29
BiPAP A40 ventilators risk therapy loss during alarm condition
BiPAP A40 ventilators may lose therapy delivery during a Ventilator Inoperative alarm, potentially causing respiratory failure or death in vulnerable patients.
Product
BiPAP A40 Ventilators: BiPAP A40, Part Numbers 1111169 (US and OUS) and (OUS ONLY)1111170 1111171 1111173 1111174 1111175 1111177 1116156 1111170S BR1111169 CN1111169 IT1111169 R1111169 R1111177 R1116156 ; BiPAP A40 Pro, Part Numbers (OUS Only): ARX3100S19
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1812-2024·2024-05-29
BiPAP V30 Auto Ventilator May Interrupt Therapy During Malfunction Alarm
Philips BiPAP V30 Auto Ventilators may interrupt or lose therapy during a Ventilator Inoperative alarm, potentially causing hypoventilation, severe oxygen depletion, or respiratory failure.
Product
BiPAP V30 Auto Ventilator, Part Number 1111178
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1253-2024·2024-05-29
Geissler's Supermarket Shrimp Tempura Recalled for Undeclared Wheat
Geissler's Supermarket is recalling Shrimp Tempura and Spicy Shrimp sushi rolls due to wheat in the tempura batter that is not declared on the label. Consumers with wheat allergies risk allergic reaction.
Product
Geissler's Supermarket Shrimp Tempura and Spicy Shrimp Ingredients read in part: "***INGREDIENTS:RICE, NORI, AVOCADO, CUCUMBER,SHRIMP TEMPURA,SHRIMP, CAYENNE PEPPER PUREE, RED JALAPENO PEPPERS, ORGANIC DRIED GARLIC, CAYENNE POWDER, XANTHAN GUM, CITRIC ACID, SOY PROTEIN, VINEGAR
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1811-2024·2024-05-29
Optum Nimbus II Plus Infusion Pump Recall Due to Potential Failure Modes
OptumHealth Care Solutions LLC is recalling 208 units of the Optum Nimbus II Plus ambulatory infusion pump distributed nationwide due to potential battery failure, system errors, and drug leakage.
Product
Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1254-2024·2024-05-29
Geissler's Supermarket Spicy Salmon Sushi Recalled for Undeclared Egg Allergen
Geissler's Supermarket is recalling Spicy Salmon sushi because the product contains egg in mayonnaise but does not declare this allergen on the label. This poses a serious risk to people with egg allergies.
Product
Geissler's Supermarket Spicy Salmon 9.6 oz Ingredients read in part: "***INGREDIENTS:RICE, NORI, AVOCADO, SALMON, MAYONNAISE, CHILI, SUGAR, SALT, GARLIC, ACETIC ACID, POTASSIUM SORBATE, SODIUM Bl SULFITE, XANTHAN GUM, VINEGAR, ORANGE JUICE, ALCOHOL, HIGH FRUCTOSE CORN SYRUP, WAT
Category
Food
Distribution
2 states
CriticalFDA (Devices)·Z-1681-2024·2024-05-22
Cardiac Catheters Recalled Due to Polyurethane Delamination and Guidewire Advancement Issues
Boston Scientific is recalling 9,271 Expo 5F Selective Angiographic Catheters due to polyurethane delamination that can prevent guidewire advancement. The defect was found in certain batches with worldwide distribution.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; cardiac catheter
Category
Medical Device
Distribution
0 states
CriticalFDA (Devices)·Z-1665-2024·2024-05-22
Expo Selective Angiographic Catheters Recalled for Material Delamination and Detachment
Boston Scientific recalls Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment that may prevent guidewire advancement during cardiac procedures. Affected batches 60443927 and 60495422 have been distributed worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (SGL), REF H749085263001; cardiac catheter
Category
Medical Device
Distribution
0 states
CriticalFDA (Devices)·Z-1671-2024·2024-05-22
Expo 5F Cardiac Catheters recalled due to polyurethane delamination
Boston Scientific recalled 2,314 Expo 5F cardiac catheters due to polyurethane delamination in the inner lining. The defect can prevent guidewire advancement during angiographic procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (SGL), REF H74908526501; cardiac catheter
Category
Medical Device
Distribution
0 states
CriticalFDA (Devices)·Z-1657-2024·2024-05-22
Boston Scientific Cardiac Catheters Recalled for Material Delamination
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to polyurethane delamination of the inner lining. The defect prevents guidewire advancement and affects 330 units worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 125CM (5PK), REF H749085262302; cardiac catheter
Category
Medical Device
Distribution
0 states
CriticalFDA (Devices)·Z-1685-2024·2024-05-22
Boston Scientific cardiac catheters recalled for delaminating polyurethane and guidewire advancement failure
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to complaints of guidewire advancement problems and polyurethane delamination in the catheter lining. Affected catheters are distributed worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 (5PK), REF H7490852624; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1647-2024·2024-05-22
Angiographic Catheters Recalled for Polyurethane Delamination and Malfunction
Boston Scientific recalls Expo 5F angiographic catheters due to polyurethane delamination and material detachment that prevents guidewire advancement. The recall affects 3,127 units in specific batches distributed worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO RCB (5PK), REF H749085261902; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1659-2024·2024-05-22
Expo selective angiographic cardiac catheters recalled for guidewire advancement failure
Boston Scientific is recalling Expo 5F selective angiographic catheters due to polyurethane layer delamination and material detachment that prevents guidewire advancement through the device.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 125CM (5PK), REF H749085262352; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1683-2024·2024-05-22
Boston Scientific cardiac catheters recalled for polyurethane delamination
Boston Scientific is recalling Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment that can prevent guidewire advancement. Approximately 37,252 catheters in specific batches are affected worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL1 (5PK), REF H74908526962; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1674-2024·2024-05-22
Expo 5F Selective Angiographic Catheters recalled for material delamination and device malfunction
Boston Scientific is recalling 1,322 Expo 5F Selective Angiographic Catheters worldwide due to polyurethane layer delamination and material detachment that prevents guidewire advancement. The defect could compromise cardiac catheterization procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (SGL), REF H74908526511; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1640-2024·2024-05-22
Expo 5F Selective Angiographic Catheters recalled due to material delamination
Boston Scientific Corporation is recalling Expo 5F Selective Angiographic Catheters in certain batches due to polyurethane layer delamination that prevents guidewire advancement. The inner lining material may detach, making the catheters unsafe to use.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 (SGL), REF H74908526031; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1656-2024·2024-05-22
Selective Angiographic Catheters Recalled Due to Material Delamination
Boston Scientific recalls Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment in the catheter lining, which may prevent guidewire advancement during medical procedures.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 125CM (5PK), REF H749085262252; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1649-2024·2024-05-22
Cardiac Catheters Recalled Due to Material Delamination and Guidewire Failure
Boston Scientific is recalling Expo 5F cardiac catheters due to material delamination in the inner lining that prevents guidewire advancement. The defect affects 25,617 units distributed worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM (5PK), REF H749085262012; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1666-2024·2024-05-22
Boston Scientific Expo 5F catheters recalled for material delamination
Boston Scientific recalls Expo 5F Selective Angiographic Catheters due to polyurethane layer delamination and material detachment that can prevent guidewire advancement. The recall affects 46,860 units distributed worldwide.
Product
Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1246-2024·2024-05-22
Infinite Herbs Organic Basil Recalled for Salmonella typhimurium Contamination
Infinite Herbs Organic Basil in 2.5 oz, 2.0 oz, and 4 oz containers has been recalled due to potential Salmonella typhimurium contamination. Approximately 235,077 units were distributed across multiple states.
Product
Infinite Herbs Organic Basil packed in a clear 2.5 oz, 2.0 oz, and 4 oz PET clamshell container.
Category
Food
Distribution
0 states

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