The Recall Desk

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.

6351–6375 of 29111

  • SevereFDA (Devices)·Z-1315-2022·2022-07-13

    Palindrome Precision Chronic Dialysis Catheters Risk Fluid Leakage Due to Hub Defect

    Covidien recalls 25,765 Palindrome Precision HSI Chronic Catheters due to a defect in the hub that may cause unintended fluid leakage during dialysis treatment.

    Product
    Palindrome Precision HSI Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1313-2022·2022-07-13

    Palindrome Precision H Chronic Catheter Recalled for Potential Hub Leakage

    Covidien is recalling certain Palindrome Precision H Chronic Catheters because the hub may leak, causing unexpected fluid to flow back during use. This FDA Class I recall affects 26,675 units distributed globally.

    Product
    Palindrome Precision H Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1403-2022·2022-07-13

    Organic Oregano Leaf Powder and Ground Oregano Recalled for Salmonella Contamination

    Pure Ground Ingredients has recalled specific lots of organic oregano leaf powder and ground oregano sold in Oregon, Wisconsin, Maryland, and Colorado due to potential Salmonella contamination.

    Product
    Pure Ground Ingredients Organic Oregano Leaf Powder Item#: OREO-PW Weight: 35 LBS/15.89 kgs Processed and Packaged at Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423 Certified Organics By CCOF Organic Oregano Leaf Ground Item#: OREO-GR Weight: 35 LBS/15.89 kgs Pro
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1276-2022·2022-07-13

    Clean Catch Urine Kit Recalled Due to Improper Assembly

    American Contract Systems is recalling 274,400 Clean Catch Urine Kits due to improper assembly by potentially untrained individuals. The FDA classified this as a Class I recall.

    Product
    Clean Catch Urine Kit NS 178489, AHMU58A
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1397-2022·2022-07-13

    Giant Eagle Peanut Butter Brownie Recalled for Salmonella Risk

    Giant Eagle is recalling a 16-ounce Peanut Butter Creme Brownie made with Jiff Peanut Butter due to potential Salmonella contamination. The product was distributed to Pennsylvania.

    Product
    GE 25135900000 Bakery, Brownie, Peanut Butter Creme 16Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1411-2022·2022-07-13

    Built Bar Banana Cream Pie Puffs Protein Bars Recalled for Potential E. coli Contamination

    Built Brands LLC is recalling approximately 4,196 individual Banana Cream Pie Puffs Protein Bars sold nationwide due to potential Escherichia coli contamination.

    Product
    Built Bar, Banana Cream Pie Puffs Protein Bar, 1.41 oz. (40 g) net wt., packaged in individual wrapper, Built Brands, LLC, 600 E Quality Dr., American Fork, UT 84003. SKU 30000318. Product sold as part of a paperboard 12-count mixed box. Each box contains 4 affected bars. UPC 8 4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V503000·2022-07-13

    2022 CAN-AM Ryker Motorcycles: Handlebar Stem Bolt Breakage Recall

    CAN-AM is recalling 2022 Ryker motorcycles due to handlebar stem bolts that may break unexpectedly, causing sudden loss of steering control and crash risk.

    Product
    CAN-AM — CAN-AM RYKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1175-2022·2022-07-13

    CVS Health Magnesium Citrate Laxative Recalled for Bacterial Contamination

    CVS Health Magnesium Citrate SALINE LAXATIVE Oral Solution (1.745 g, Lemon Flavor, 10 FL OZ) is being recalled due to microbial contamination with Gluconacetobacter Liquefaciens. Approximately 98,958 bottles distributed nationwide are affected.

    Product
    CVS Health Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon Flavor, 10 FL OZ (296 mL), Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 30594 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1398-2022·2022-07-13

    Giant Eagle Chocolate Peanut Butter Cake Recalled for Salmonella Risk

    Giant Eagle is recalling chocolate peanut butter iced cakes made with Jiff Peanut Butter due to potential Salmonella contamination. The product was distributed in Pennsylvania.

    Product
    GE 25136000000 Bakery, Cake, Chocolate, Peanut Butter Iced 8Oz 4
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1320-2022·2022-07-13

    Dialysis Catheters Recalled for Potential Fluid Leakage from Hub Defect

    Covidien is recalling Mahurkar Chronic Carbothane dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use. Approximately 132,443 units distributed worldwide are affected.

    Product
    Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1393-2022·2022-07-13

    Giant Eagle Torte Peanut Butter Recalled for Potential Salmonella Contamination

    Giant Eagle Torte Peanut Butter (62 oz, code GE 23984200000) is recalled due to potential Salmonella contamination from the Jiff peanut butter ingredient. Consumers should not consume this product.

    Product
    GE 23984200000 Torte Peanut Butter 62Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1396-2022·2022-07-13

    Giant Eagle Peanut Butter Fudge Split Cake Recalled for Potential Salmonella

    Giant Eagle's Peanut Butter Fudge Split Cake, made with Jiff Peanut Butter, is being recalled due to potential Salmonella contamination. The recall affects units distributed in Pennsylvania.

    Product
    GE 25115700000 Bakery, Cake, Peanut Butter Fudge Split 25.6 Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1277-2022·2022-07-13

    COVID-19 nasopharyngeal sample collection tray recalled due to improper assembly

    American Contract Systems, Inc. recalls 274,400 COVID-19 test kits distributed in Minnesota due to off-site assembly by individuals who may not have been properly trained.

    Product
    Nasopharyngeal sample collection tray for COVID-19 testing, labeled as COVID TEST KIT NONSTERILE 184312, AHCV18A
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-1388-2022·2022-07-13

    Organic oregano ground recalled due to Salmonella contamination

    OS Holding Inc is recalling Organic Oregano Ground distributed in Arizona, Minnesota, and Wisconsin due to potential Salmonella leeuwarden contamination.

    Product
    Organic Oregano Ground is packed in bulk 35 lbs. cases with food-grade poly bag that is labeled in parts: "OREGONSPICE COMPANY***OG Oregano Ground***Net Wt 35 lb (15.89 kg)***13320 NE Jarrett St.*Portland, Oregon 97230***".
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1316-2022·2022-07-13

    Palindrome Chronic Catheter recalled due to potential hub leakage

    Covidien is recalling Palindrome Chronic Catheters due to a potential leaking condition in the hub that may cause unexpected fluid return during use.

    Product
    Palindrome Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1395-2022·2022-07-13

    Giant Eagle Peanut Butter Fudge Bar Cake Recalled for Salmonella Risk

    Giant Eagle is recalling Peanut Butter Fudge Bar Cake made with Jiff Peanut Butter due to potential Salmonella contamination. The affected product was distributed in Pennsylvania.

    Product
    GE 25022900000 Peanut Butter Fudge Bar Cake 22.6 Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1394-2022·2022-07-13

    Giant Eagle Brownie Classic Peanut Butter Recalled for Potential Salmonella

    Giant Eagle Brownie Classic Peanut Butter is recalled due to potential Salmonella contamination from the Jiff Peanut Butter ingredient. Affected product distributed in Pennsylvania.

    Product
    GE 24777800000 Brownie Classic Peanut Bttr 8c , 14Oz
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1317-2022·2022-07-13

    Palindrome H Chronic Catheters Recalled for Potential Hub Leaking

    Palindrome H Chronic Catheters are being recalled due to a potential leaking condition in the catheter hub that may result in unanticipated fluid return during hemodialysis treatment. Affected units have been distributed worldwide.

    Product
    Palindrome H Chronic Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V501000·2022-07-13

    2022 Toyota Tundra rear camera software defect increases crash risk

    The 2022 Toyota Tundra with Panoramic View Monitor may display front camera footage instead of rear camera when in reverse, reducing rear visibility and increasing crash risk. Toyota will reprogram the parking assist system free of charge.

    Product
    TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1312-2022·2022-07-13

    Palindrome Precision Chronic Dialysis Catheter Hub Leak Risk

    Palindrome Precision Chronic Catheters used for dialysis may leak due to a flaw in the hub component, potentially allowing unintended fluid to escape during treatment.

    Product
    Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V499000·2022-07-12

    Vermeer Recalls 2022 BC1800XL Trailers Due to Hitch Bolt Defect

    Vermeer is recalling 2022 BC1800XL trailers because improper hitch bolts may fail, causing the trailer to separate and increasing crash risk.

    Product
    VERMEER — VERMEER BC1800XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V495000·2022-07-11

    Prevost Recalls 2021 X3-45 Commuter Buses Due to Missing Seat Bolt

    Prevost is recalling 30 units of the 2021 X3-45 commuter bus because a bolt securing the rear bench seat was not installed, creating a crash injury risk.

    Product
    PREVOST — PREVOST X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide