The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

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.

1051–1075 of 7439

  • CriticalFDA (Food)·F-0234-2024·2023-03-22

    Strawberry Yogurt Parfaits Recalled for Potential Listeria Contamination

    Fresh Creative Cuisine is recalling 9-ounce strawberry yogurt parfaits distributed across 11 states due to potential Listeria monocytogenes contamination. Products were sold January 24-30, 2023.

    Product
    Fresh Creative Cuisine White Label, Strawberry Low Fat Yogurt, Fruit & Granola Parfait, Net Wt. 9 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0164-2024·2023-03-22

    Quick & Fresh Italian Finger Sandwiches recalled for potential Listeria contamination

    FRESH IDEATION FOOD GROUP, LLC is recalling Quick & Fresh Italian Finger Sandwiches due to potential Listeria monocytogenes contamination in products sold January 24–30, 2023 across 11 states.

    Product
    Quick & Fresh, Italian Finger Sandwiches, Net . Wt. 6.5 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0530-2023·2023-03-22

    Cranberry Chicken Salad Brioche Recalled for Listeria Contamination Risk

    Fresh Creative Cuisine is recalling Cranberry Chicken Salad Brioche products sold January 24-30, 2023 due to potential Listeria monocytogenes contamination. Affected states include MD, PA, DE, NY, DC, NJ, NC, CT, SC, VA, and MA.

    Product
    Fresh Creative Cuisine, Cranberry Chicken Salad Brioche, Net . Wt. 7.6 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0194-2024·2023-03-22

    Quick & Fresh Turkey Sandwich Recalled for Potential Listeria Contamination

    Fresh Ideation Food Group is recalling Quick & Fresh Peppered Turkey & Havarti sandwiches due to potential Listeria monocytogenes contamination. The affected products were distributed in January 2023 across multiple eastern states.

    Product
    Quick & Fresh, Peppered Turkey & Havarti on Oat Roll, Net . Wt. 8.25 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0473-2023·2023-03-22

    Bistro To Go Crudite Salad Recalled for Listeria Contamination Risk

    Fresh Ideation Food Group is recalling Bistro To Go Crudite & Chipotle Ranch Dressing products distributed across eleven states due to potential Listeria monocytogenes contamination.

    Product
    Bistro To Go, Crudite & Chipotle Ranch Dressing, Net Wt. 6.5 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-0285-2024·2023-03-22

    Fresh Creative Cuisine Yogurt Recalled for Potential Listeria Contamination

    Fresh Creative Cuisine Black Label vanilla yogurt cups are recalled due to potential Listeria monocytogenes contamination. The 9 oz. single-serving products sold between January 24-30, 2023 were distributed across 11 states.

    Product
    Fresh Creative Cuisine Black Label, Vanilla Low Fat Yogurt, Mixed Berries & Granola, Net Wt. 9 Oz. Single Serving, Keep refrigerated
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Devices)·Z-1148-2023·2023-03-15

    Cardiosave Rescue intra-aortic balloon pump may shut down unexpectedly

    The Cardiosave Rescue intra-aortic balloon pump may suddenly stop working due to communication failure between internal circuit boards, interrupting patient therapy and threatening hemodynamic stability.

    Product
    Cardiosave Rescue Model Nos. 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0455-2023·2023-03-15

    Hand Sanitizer Recalled for Methanol and Acetaldehyde Contamination

    Snowy Range Blue hand sanitizer is recalled due to FDA findings of methanol, acetaldehyde, and acetal above permissible limits. The product was distributed nationwide across all lot codes.

    Product
    Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·23150·2023-03-09

    Calico Critters Animal Figures Recalled Due to Choking Hazard; Two Deaths Reported

    Epoch Everlasting Play is recalling more than 3.2 million Calico Critters animal figures and sets sold with bottle and pacifier accessories due to choking hazard. Two fatal incidents have been reported.

    Product
    Calico Critters® Animal Figures and Sets sold with Bottle and Pacifier Accessories
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0370-2023·2023-03-01

    Harvest Sesame Recalled for Undeclared Soy and Sesame Allergens

    Daiso is recalling Harvest Sesame 94g units due to undeclared soy and sesame allergens on the label. The recall affects 317,751 units distributed across Daiso retail locations in six U.S. states and Canada.

    Product
    Harvest Sesame 94g units UPC:4901940041312
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0374-2023·2023-03-01

    Daiso: Fly Beans Senbei cracker recall due to unlabeled peanuts

    Daiso is recalling KASHIWADO Hitoritoiro Fly Beans Senbei because the product contains peanuts not listed on the label, creating a risk for consumers with peanut allergies.

    Product
    KASHIWADO Hitoritoiro Fly Beans Senbei UPC:4904036008213
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0371-2023·2023-03-01

    Harvest Biscuits recalled for undeclared soy and peanut allergens

    Harvest Biscuits 4Kinds of Nuts (94g units) are recalled because the product contains soy and peanuts that are not listed on the ingredient label. The product was distributed to Daiso stores across multiple US states and Canada.

    Product
    Harvest Biscuits 4Kinds of Nuts 94g units UPC:4901940041558
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0402-2023·2023-03-01

    Ready-to-Eat Soup Recalled: Rao's Contains Undeclared Egg Allergen

    Rao's Made for Home Slow Simmered Soup labeled as Chicken & Gnocchi is being recalled because it actually contains vegetable minestrone with an undeclared egg allergen. The recall affects 13,751 cases distributed across multiple states.

    Product
    Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrigerate after opening.
    Category
    Food
    Distribution
    12 states
  • CriticalCPSC·23136·2023-02-23

    LumaRail Bed Assist Rails recalled for entrapment and asphyxia hazard

    Platinum Health is recalling about 53,000 LumaRail bed assist rails because users can become entrapped between the rail and mattress, risking death by asphyxiation. One death has been reported.

    Product
    LumaRail Bed Assist Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1056-2023·2023-02-15

    GE Nuclear Medicine Imaging Systems detector fall hazard

    GE Nuclear Medicine 600/800 series imaging systems may have faulty detectors that could fall, causing serious injury. Mitigation measures may not be properly implemented on 34 units distributed worldwide.

    Product
    GE Nuclear Medicine 600/800 series systems, specifically: a) OPTIMA O640 X 3/8 inch NR, b) DISCOVERY O640 X 3/8 inch, c) NM OPTIMA O640 X 3/8 inch, d) O640 NM Gantry 3/8 inch, e) O640 NM GANTRY FINAL ASSY, f) OPTIMA O640 X 3/8 inch; Emission Computed Tomography System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0246-2023·2023-02-08

    First Aid Kit with Burn Cream Recalled for Bacterial Contamination

    GFA Production is recalling Adventure First Aid 1.0 kits containing Easy Care After Burn Cream due to confirmed bacterial contamination found in FDA testing. The affected product was distributed nationwide and in Canada.

    Product
    Adventure First Aid 1.0, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0213
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0244-2023·2023-02-08

    Easy Care first aid burn cream recalled for microbial contamination

    Easy Care first aid burn cream distributed nationwide and in Canada is recalled due to FDA-detected contamination with Bacillus lichenformis and Bacillus sonorensis. The product should not be used.

    Product
    Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and lidocaine hydrochloride 0.5%), 0.9 g (0.03 oz) packets packaged in boxes of 10, Treatment for Burns, Made in China for Adventure Ready Brands, 944 Industrial Park Rd., Littleton, NH 03561, NDC 90107-0210, Product # 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0250-2023·2023-02-08

    Easy Care First Aid Kit Recalled for Bacterial Contamination

    GFA Production is recalling Easy Care First Aid Kits distributed nationwide and in Canada due to bacterial contamination of included After Burn Cream packets. The FDA confirmed the presence of Bacillus lichenformis and Bacillus sonorensis.

    Product
    Easy Care First Aid Class A ANSI 25 Person, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2150
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0184-2023·2023-02-01

    Vancomycin Hydrochloride Injection Recalled for Glass Particulate Matter

    Pfizer recalls approximately 89,700 vials of Vancomycin Hydrochloride for Injection due to glass particulate matter contamination. The recalled product (Lot 33045BA) was distributed across the USA and Puerto Rico.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0296-2023·2023-01-25

    Dough Ball Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling Greco and Sons Dough Room dough ball products because they contain undeclared milk allergen, which poses a serious risk to milk-allergic consumers.

    Product
    Greco and Sons Dough Room Product No. 9009 Teresa's 9 oz.; Greco and Sons Dough Room Product No. 9012 Teresa's 12 oz.; Greco and Sons Dough Room Product No. 9020 Teresa's 22 oz.; Greco and Sons Dough Room Product No. 9046 Teresa's 48 oz.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Devices)·Z-0886-2023·2023-01-25

    Cardiosave IABP may shut down unexpectedly due to blood contamination

    The Cardiosave Rescue Intra-Aortic Balloon Pump may shut down unexpectedly if blood enters the device through a compromised balloon catheter. Approximately 46 units have been distributed worldwide.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85, 0998-UC-0800-75, 0998-UC-0800-83, 0998-UC-0800-85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·23088·2023-01-09

    Fisher-Price Recalls 4.7 Million Rock 'n Play Sleepers Due to Infant Deaths

    Fisher-Price is recalling approximately 4.7 million Rock 'n Play Sleepers after at least 8 deaths were reported following the initial April 2019 recall announcement. Infants have died after rolling from their back to their stomach or side while unrestrained.

    Product
    All models of Rock 'n Play Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·23089·2023-01-09

    Kids2 Rocking Sleepers Recalled After 15 Infant Deaths

    Kids2 is recalling approximately 694,000 Rocking Sleepers after 15 infant fatalities were reported. Infants died after rolling from their back to their stomach or side while unrestrained.

    Product
    All models of Kids2 Rocking Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·045-2022·2022-12-22

    Morasch Meats Recalls Raw Frozen Diced Beef Due to E. Coli O157:H7

    Morasch Meats is recalling approximately 3,930 pounds of raw frozen diced beef products produced on August 24, 2022, due to possible E. coli O157:H7 contamination.

    Product
    Morasch Meats, Inc — Morasch Meats Inc. Recalls Raw Frozen Diced Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·23078·2022-12-22

    Target Recalls Pillowfort Weighted Blankets Due to Asphyxiation Risk

    Target is recalling about 204,000 Pillowfort Weighted Blankets because children can become entrapped inside the blanket cover, creating a risk of asphyxiation. Two children have died from this hazard.

    Product
    Pillowfort™ Weighted Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide