The Recall Desk

Archive

May 2023 recalls

754 recalls were announced in May 2023.

What the numbers show

Critical
15
Severe
132
High
528
Moderate
72
Low
7

Of the 754 recalls this month scored against our rubric, 2% are Critical, 18% are Severe.

401–500 of 754

  • ModerateCPSC·23757·2023-05-18

    Shimano PRO Vibe Alloy Bicycle Stems Recalled for Crack and Injury Risk

    Shimano is recalling about 400 PRO Vibe Alloy stems for road bicycles because the stems can crack and break during use, causing loss of control and crash risk. Two reports of cracking have been received in the U.S., but no injuries have been reported.

    Product
    Shimano PRO Vibe Alloy stems for road bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23758·2023-05-18

    Cole & Mason Pepper Mills Recalled for Metal Shard Laceration Hazard

    DKB Household is recalling Cole & Mason 505WEG Pepper Mills due to a metal grinding mechanism that sheds metal shards during initial use, posing a laceration risk. No injuries have been reported.

    Product
    Cole & Mason 505WEG Pepper Mills Item Number H50501PWE
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23206·2023-05-18

    Kell Electronic Personal Chiller Mini Refrigerators Recalled for Burn Hazard

    Kell Electronic is recalling about 25,000 Personal Chiller Mini Fridge Gamer Beverage Refrigerators with LED Lights because the power cord can overheat and cause burns. No injuries have been reported.

    Product
    Personal Chiller Mini Fridge Gamer Beverage Refrigerators with LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0839-2023·2023-05-17

    Meijer Chicken BLT Salad Recalled for Listeria Contamination

    Meijer is recalling Fresh From Meijer Chicken BLT Salad due to potential Listeria monocytogenes contamination. Affected products were distributed in six Midwestern states with sell-by dates of March 20-27, 2023.

    Product
    Fresh From Meijer Chicken BLT Salad 8.2 Oz UPC - 719283679307
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0833-2023·2023-05-17

    Meijer Avocado Chicken Bacon Ranch Salad Recalled for Listeria Risk

    Meijer is recalling Fresh From Meijer Avocado Chicken Bacon Ranch Salad due to potential Listeria monocytogenes contamination. The affected products were sold at Meijer stores in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Avocado Chicken Bacon Ranch Salad 8 Oz UPC - 713733246118
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0826-2023·2023-05-17

    Revolution Farms spring mix recalled for listeria contamination

    Revolution Farms Michigan Spring Mix and Farmer's Mix products distributed in Michigan, Ohio, and Wisconsin are recalled due to potential Listeria monocytogenes contamination.

    Product
    Revolution Farms Michigan Spring Mix plastic 5oz Retail container UPC 856791008004 and 3lb bulk clear poly bag UPC 856791008042 Revolution Farms Farmer's Mix 3lb bulk clear poly bag UPC 856791008134
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0825-2023·2023-05-17

    Revolution Farms Great Lakes Gourmet recalled for Listeria contamination

    Revolution Farms is recalling Great Lakes Gourmet products due to potential Listeria monocytogenes contamination. The recall affects products distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Great Lakes Gourmet plastic 5oz Retail container UPC 856791008028 and 3lb bulk clear poly bag UPC 856791008066
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-1496-2023·2023-05-17

    Cordis Angioguard Emboli Capture Guidewire System Faces Separation Hazard

    Cordis's Angioguard RX/XP Emboli Capture Guidewire System is recalled due to potential separation of the delivery system and capture sheath, which could cause procedural delays, unplanned intervention, or stroke during use.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RE
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·F-0838-2023·2023-05-17

    Fresh From Meijer Southwest Chicken Salad Recalled for Listeria Monocytogenes

    Meijer Inc. is recalling Fresh From Meijer Southwest Chicken Salad due to potential Listeria monocytogenes contamination. The product was distributed in six Midwestern states.

    Product
    Fresh From Meijer Southwest Chicken Salad 8.8 Oz UPC - 760236488323
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0837-2023·2023-05-17

    Fresh From Meijer Michigan Harvest Salad Recalled Due to Listeria Contamination

    Meijer Inc. is recalling Fresh From Meijer Michigan Harvest Salad (6.7 oz) due to Listeria monocytogenes contamination. About 2,492 units with sell-by dates from March 22-29, 2023 were distributed in six states.

    Product
    Fresh From Meijer Michigan Harvest Salad 6.7 Oz UPC - 719283679291
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1487-2023·2023-05-17

    Emboli Capture Guidewire System Separation Hazard Prompts FDA Recall

    The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate from its delivery sheath during medical procedures, potentially causing stroke or requiring emergency surgery. Cordis US Corp is recalling 146 units worldwide.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0834-2023·2023-05-17

    Meijer Tomato Caprese Salad Recalled Due to Listeria Risk

    Meijer is recalling Fresh From Meijer Tomato Caprese Salad due to potential Listeria monocytogenes contamination. The product was distributed to stores across six states.

    Product
    Fresh From Meijer Tomato Caprese Salad 6 Oz UPC - 713733246101
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1490-2023·2023-05-17

    ANGIOGUARD RX/XP Emboli Capture Guidewire System May Separate During Procedures

    ANGIOGUARD RX/XP emboli capture guidewire systems may separate from their delivery sheaths during interventional procedures, potentially causing stroke. Cordis is recalling 56 units distributed worldwide.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·23V349000·2023-05-17

    Foretravel Recalls 2022-2024 Motorhomes Due to Software Error

    Foretravel is recalling 2022-2024 Realm, FS450, and Realm Presidential motorhomes because a software error may cause loss of drive power or disable safety systems.

    Product
    FORETRAVEL — FORETRAVEL REALM, FS450, REALM PRESIDENTIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0828-2023·2023-05-17

    Revolution Farms Salad Kits Recalled for Listeria Contamination

    Revolution Farms is recalling Traverse City Cherry 6-ounce salad kits due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Traverse City Cherry 6oz salad kit in plastic container UPC 856791008226
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0832-2023·2023-05-17

    Meijer Chicken Cobb Salad Recalled Due to Listeria Contamination Risk

    Meijer Inc. is recalling Fresh From Meijer Chicken Cobb Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in six states.

    Product
    Fresh From Meijer Chicken Cobb Salad 8.8 Oz UPC - 719283679321
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0823-2023·2023-05-17

    Revolution Farms Green Sweet Crisp Recalled for Listeria monocytogenes

    Revolution Farms is recalling Green Sweet Crisp and Sweet Crisp Deli Leaf products from Michigan, Ohio, and Wisconsin due to potential Listeria monocytogenes contamination. Consumers should not eat and should discard affected products.

    Product
    Revolution Farms Green Sweet Crisp plastic 5oz Retail container UPC 856791008141 and 3lb bulk clear poly bag UPC 856791008172 Revolution Farms Sweet Crisp Deli Leaf plastic 5oz Retail container UPC 856791008189
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0876-2023·2023-05-17

    FDA Recalls Kimura Burdock Salt for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Kimura burdock salt because it contains fish (sardines, bonito, tuna) not listed on the label. People with fish allergies may have a serious allergic reaction.

    Product
    Kimura burdock salt 40g UPC: 4972304293524
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0871-2023·2023-05-17

    Takuma Herb Salt Peanuts Recalled for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Takuma food herb salt peanuts because the product contains fish (Bonito, Sardines, Tuna) but does not list it on the label. Consumers with fish allergies could unknowingly consume the product.

    Product
    Takuma food herb salt peanut 80g UPC: 4962679652767
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0841-2023·2023-05-17

    Vitamin B Capsules Recalled for Undeclared Milk Allergen

    EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.

    Product
    Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles under the following brands: 1. EuroMedica Active B Complex, Product #68006, UPC 3 67703 68006 0. Manufactured by a cGMP compliant facility exclusively for: Eur
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0831-2023·2023-05-17

    Meijer Chicken Caesar Salads Recalled Due to Listeria monocytogenes Contamination

    Meijer Inc. is recalling Fresh From Meijer Chicken Caesar Salads (6.4 oz and 10 oz sizes) due to potential Listeria monocytogenes contamination. Products were distributed to Meijer stores in six states: Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Chicken Caesar Salad 6.4 Oz UPC - 760236117452 Fresh From Meijer Chicken Caesar Shareable Salad 10 Oz UPC - 719283679338
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0827-2023·2023-05-17

    Revolution Farms Sesame Ginger Crunch Salad Kit Recalled for Listeria Monocytogenes

    Revolution Farms Sesame Ginger Crunch 6oz salad kits (UPC 856791008233, 'Sell By 3/23/23') are recalled due to potential Listeria monocytogenes contamination. Affected units were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Sesame Ginger Crunch 6oz salad kit in plastic container UPC 856791008233
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1489-2023·2023-05-17

    Emboli Capture Guidewire System recalls risk of device separation during procedures

    Cordis is recalling an emboli capture guidewire system due to potential separation of components during medical procedures. The separation could cause procedural delays, unplanned interventions, or stroke.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1428-2023·2023-05-17

    Cook Blue Rhino G2 Tracheostomy Introducer Trays Recalled for Connection Defect

    Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because the device connectors are not making secure connections with 15mm caps and other circuit components, resulting in unsecure connections.

    Product
    Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Reference Part Numbers C-PTISYJ-100-HC-G-EU-FLEX8.5 (G57725), C-PTISYJ-100-HC-G-NA-FLEX7.5 (G57720), C-PTISYJ-100-HC-G-NA-FLEX8.5 (G57721), C-PTISY-100-HC-G-NA-FLEX8.5 (G57717), C-PTISY-100-HC-G-NA-FLEX7.5 (G57716)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1485-2023·2023-05-17

    ANGIOGUARD RX/XP Guidewire System May Separate During Medical Procedures

    The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate during medical procedures, potentially delaying treatment or requiring unplanned intervention. The recall affects 471 units distributed worldwide.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0835-2023·2023-05-17

    Meijer Mediterranean Salad Recalled Due to Listeria Contamination

    Meijer Inc is recalling Fresh From Meijer Mediterranean Salad due to potential Listeria monocytogenes contamination. Approximately 1,064 units were distributed to Meijer stores in six Midwest states.

    Product
    Fresh From Meijer Mediterranean Salad - 6.5 Oz UPC - 713733246132
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1495-2023·2023-05-17

    Emboli Capture Guidewire System Separation Risk Recalls ANGIOGUARD RX/XP

    Cordis US Corp is recalling ANGIOGUARD RX/XP Emboli Capture Guidewire Systems worldwide due to potential separation of the delivery system and capture sheath during procedures, which could cause stroke or require emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0829-2023·2023-05-17

    Revolution Farms Salad Kit Recalled for Listeria Contamination

    Revolution Farms Zesty Southwest salad kits are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Zesty Southwest 6oz salad kit in plastic container UPC 856791008240
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1486-2023·2023-05-17

    Emboli Capture Guidewire System Recalled Due to Potential Component Separation

    Cordis US Corp recalls 54 units of the ANGIOGUARD RX/XP Emboli Capture Guidewire System due to potential separation of device components. This could delay procedures or result in unplanned intervention, including possible stroke.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1488-2023·2023-05-17

    FDA Class I Guidewire System Recalled for Device Separation Risk

    Cordis US Corp is recalling the ANGIOGUARD RX / XP Emboli Capture Guidewire System because the device may separate during procedures, risking stroke or requiring emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1492-2023·2023-05-17

    ANGIOGUARD Emboli Capture Guidewire System Recalled Due to Device Separation

    The FDA has recalled the ANGIOGUARD RX/XP Emboli Capture Guidewire System because the delivery system and capture sheath could separate during use, potentially causing stroke or requiring emergency surgery.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0824-2023·2023-05-17

    Revolution Farms Romaine Lettuce Recalled for Listeria Contamination

    Revolution Farms romaine lettuce products distributed in Michigan, Ohio, and Wisconsin are recalled due to potential Listeria monocytogenes contamination. Consumers should not consume affected products and should discard them.

    Product
    Revolution Farms Robust Romaine plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1483-2023·2023-05-17

    ANGIOGUARD RX / XP Emboli Capture Guidewire System separation during procedures

    The ANGIOGUARD RX / XP emboli capture guidewire system may separate from its delivery sheath during medical procedures, potentially leading to stroke or complications requiring emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0567-2023·2023-05-17

    Atovaquone Oral Suspension Recalled for Bacillus cereus Contamination

    Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.

    Product
    ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1493-2023·2023-05-17

    ANGIOGUARD Emboli Capture Guidewire System recalled due to potential device separation

    Cordis US Corp's ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled by the FDA (Class I) because the delivery system and capture sheath may separate during medical procedures, potentially requiring emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1494-2023·2023-05-17

    Emboli Capture Guidewire System recalled for component separation risk

    The ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled because the delivery system and capture sheath may separate during procedures, potentially causing stroke or requiring emergency surgical intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0836-2023·2023-05-17

    Fresh From Meijer Shareable Garden Salad Recalled for Listeria

    Fresh From Meijer Shareable Garden Salad 11.5 oz is being recalled due to potential Listeria monocytogenes contamination. The recall affects salads distributed to Meijer stores across six states with a sell-by date of 3/31/2023.

    Product
    Fresh From Meijer Shareable Garden Salad 11.5 Oz UPC - 713733295376
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0840-2023·2023-05-17

    Salad Product Recalled by Meijer for Listeria Contamination

    Meijer Inc is recalling Fresh From Meijer Cranberry Spinach Shareable Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Cranberry Spinach Shareable Salad 12 Oz UPC - 708820304321
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1427-2023·2023-05-17

    Blue Rhino G2 Tracheostomy Introducer Sets Recalled for Unsecure Connections

    Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets due to unsecure connections with 15mm caps and circuit components that may disconnect during medical procedures.

    Product
    Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set, Reference Part Numbers C-PTIS-100-HC-G-EU-FLEX7.5 (G57695), C-PTIS-100-HC-G-EU-FLEX8.5 (G57696), C-PTIS-100-HC-G-NA-FLEX7.5 (G57691), C-PTIS-100-HC-G-NA-FLEX8.5 (G57692)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1491-2023·2023-05-17

    Emboli Capture Guidewire System recalled due to potential device separation

    Cordis US Corp is recalling the ANGIOGUARD RX/XP Emboli Capture Guidewire System (1,087 units worldwide) due to potential separation of the delivery system and capture sheath, which could lead to stroke.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0867-2023·2023-05-17

    Daisho Crab Miso Soup Recalled for Missing Shrimp Allergen Warning

    Daisho crab miso soup is being recalled because the product contains shrimp but the label warns only for crab, posing a risk to consumers with shrimp allergies. Products were distributed across multiple US states and Canada.

    Product
    Daisho crab miso soup 750g UPC: 4904621043919
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0822-2023·2023-05-17

    Dr. Rico Perez Super Kids Colostrum Dietary Supplement Recalled for Undeclared Milk Allergen

    Dr. Rico Perez Super Kids Colostrum chewable tablets are being recalled because the product contains milk but does not declare this allergen on the label. Consumers with milk allergies may be at risk.

    Product
    Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0859-2023·2023-05-17

    Sunrise Mimosa chocolate recalled for undeclared soy, milk, and tree nuts

    Windy Hill Chocolate LLC is recalling Sunrise Mimosa chocolate due to undeclared allergens: soy, milk, and tree nuts. Consumers with allergies or sensitivities to these ingredients should not consume this product.

    Product
    Sunrise Mimosa
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0857-2023·2023-05-17

    Raspberry Products Recalled for Undeclared Soy, Milk, and Tree Nut Allergens

    Windy Hill Chocolate LLC is recalling raspberry products due to undeclared soy, milk, and tree nut allergens. Products with batch number 0120230121 and expiration date 4/12/23 may contain these allergens not listed on packaging.

    Product
    Raspberry
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0844-2023·2023-05-17

    Caramel Rum Truffle Recalled for Undeclared Soy, Milk, and Tree Nut Allergens

    Windy Hill Chocolate LLC is recalling Caramel Rum Truffle candies (Batch #1023220097) for undeclared soy, milk, and tree nut allergens. Affected consumers should not consume the product if they have allergies to these ingredients.

    Product
    Caramel Rum Truffle
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0879-2023·2023-05-17

    Kurata Foods Vegetable Potage V Ramen recalled for unlisted coconut allergen

    DAISO CALIFORNIA WAREHOUSE is recalling Kurata Foods Vegetable Potage V Ramen because coconut was not listed in the ingredients or allergen statement. The product was distributed across multiple U.S. states and British Columbia Canada.

    Product
    Kurata Foods Vegetable Potage V Ramen 2 servings UPC: 4906436005304
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1578-2023·2023-05-17

    Sheath Introducer Kit with Incorrect Needle Size Recalled

    Merit Medical Systems is recalling COBRA-OS Sheath Introducer Kits due to an incorrect needle size that may affect proper insertion during medical procedures.

    Product
    COBRA-OS, custom Sheath Introducer Kit, 4 French, REF: E01P2, Sterile EO, Single Use, RX Only, 5 Units
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0863-2023·2023-05-17

    Dried squid snack recalled for undeclared fish allergen

    DAISO dried squid snack recalled because fish other than squid is present but not listed in ingredients or allergen statement. Consumers with fish allergies are at risk.

    Product
    Pacifier dried squid cut sea urchin soy sauce flavor 20g UPC: 4904523229343
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0853-2023·2023-05-17

    Chocolate Covered Oreos recalled for undeclared soy, milk, and tree nut allergens

    Windy Hill Chocolate LLC is recalling Chocolate Covered Oreos due to undeclared soy, milk, and tree nut allergens. The product was distributed domestically and poses a risk to consumers with allergies to these ingredients.

    Product
    Chocolate Covered Oreos
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0849-2023·2023-05-17

    Hazelnut Crunch Recalled for Undeclared Allergens: Soy, Milk, Tree Nuts

    Windy Hill Chocolate LLC is recalling Hazelnut Crunch (batch #1119220112) due to undeclared allergens: soy, milk, and tree nuts. Consumers with allergies to these ingredients should not consume the product.

    Product
    Hazelnut Crunch
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0865-2023·2023-05-17

    Mangetsu Ebisen Crackers Recalled for Undeclared Krill Allergen

    Mangetsu Ebisen 54g crackers are recalled because krill is present in the product but not listed in the ingredients statement, only in a general shellfish warning.

    Product
    Mangetsu Ebisen 54g UPC: 4901053011370
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0880-2023·2023-05-17

    Fujiya Country Ma'am Snacks Recalled for Undisclosed Peanut Allergen

    Daiso California Warehouse is recalling Fujiya Country Ma'am Vanilla & Cocoa wafers because they contain peanut (sheanut) that is not declared on the label. Consumers with peanut allergies should not consume this product.

    Product
    Fujiya Country Ma'am Vanilla & Cocoa 19 sheets UPC: 4902555272641
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0850-2023·2023-05-17

    Key Lime Bonbon Recalled for Undeclared Soy, Milk, Tree Nuts

    Windy Hill Chocolate LLC recalls Key Lime Bonbons due to undeclared allergens (soy, milk, tree nuts). Consumers with allergies should not consume this product.

    Product
    Key Lime Bonbon
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1571-2023·2023-05-17

    PDS Plus Antibacterial Suture Potential Breakage During Intraoperative Use

    Ethicon recalled 1,656 units of PDS Plus Antibacterial Suture due to potential breakage during surgery, which could compromise tissue approximation. The affected lot was distributed to the United Kingdom, Ireland, and Turkey.

    Product
    PDS¿ Plus Antibacterial (polydioxanone) Suture - PDS PLUS CLR 27IN(70CM) USP3-0(M2) S/A PC-25 PRIME. Intended for use in general soft tissue approximation, including use in pediatric cardiovascular tissue. Product Code: PDP9625H
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0861-2023·2023-05-17

    Ajikal Kotsubukko Snack Recalled for Undeclared Coconut

    Ajikal 44g Kotsubukko snacks containing undeclared coconut were distributed across multiple US states and Canada. Consumers with a coconut allergy should not consume this product.

    Product
    Ajikal 44g Kotsubukko 4 series UPC: 4510656600708
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1573-2023·2023-05-17

    Laboratory Management Software May Display Incorrect Slide Labels

    TDHisto/Cyto laboratory management software may display incorrect information on slide labels in specific use cases. The FDA has issued a Class II recall affecting laboratories nationwide in California.

    Product
    TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological and gynecological cytology and autopsy activities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0830-2023·2023-05-17

    Ziyad Cinnamon Powder Recalled for Elevated Lead Levels

    ZB Importing LLC is recalling Ziyad cinnamon powder (4.5 oz jars) from lot 21321G2 due to elevated lead levels. The recall affects 3,456 units distributed across multiple U.S. states and territories.

    Product
    Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1575-2023·2023-05-17

    STA R Max Analyzer Firmware Bug Produces Inaccurate Coagulation Test Results

    Diagnostica Stago is recalling the STA R Max fully automatic clinical analyzer due to a firmware bug that causes intermittent shortened coagulation times and increased technical errors, potentially producing inaccurate blood clotting test results.

    Product
    STA R Max fully automatic clinical instrument designed to perform tests on human plasmas, Reference Numbers 59013 and 59026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0860-2023·2023-05-17

    Ajikal Age Ichiban Snack Recalled for Undeclared Coconut Allergen

    Ajikal Age Ichiban 97g snacks are being recalled due to undeclared coconut, a tree nut allergen that can cause allergic reactions. The affected product was distributed across multiple US states and Canada.

    Product
    Ajikal Age Ichiban 97g UPC: 4510656600906
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1579-2023·2023-05-17

    BD Pyxis MedStation ES software failure causes patient data loss

    BD Pyxis automated dispensing cabinet software versions 1.7.0 through 1.7.4 experience download failures causing partial loss of patient information and transaction data. This may result in dispensing incorrect medication doses, allergenic medications, or discontinued medications.

    Product
    BD Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES (Med ES Main Tower), REF: 352; BD Pyxis Anesthesia Station ES, REF: 327; BD Pyxis CII Safe ES Tower Main, REF: 1116-00; BD Pyxis CII Safe ES, Desktop PC, W-LESS SCNR, BIO, REF: 107-255-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0874-2023·2023-05-17

    Kajitani Food Congeri Crispy recalled due to undeclared coconut allergen

    Kajitani Food Congeri Crispy crackers (104g, UPC 4901332108661) contain coconut but do not list it in the ingredients or allergen statement. Consumers with coconut allergies may be at risk; approximately 2,199 units were distributed to retail locations across multiple US states and Canada.

    Product
    Kajitani Food Congeri Crispy 104g UPC: 4901332108661
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0873-2023·2023-05-17

    Kanro Non-Sugar Tea House Recalled for Undeclared Coconut Allergen

    Kanro Non-Sugar Tea House 40g has been recalled because coconut allergen is not listed in the product ingredients. Consumers with coconut allergies should not consume this product.

    Product
    Kanro Non-Sugar Tea House 40g UPC: 4901351013144
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1574-2023·2023-05-17

    Medtronic Spinal Distractor Rack Recalled for Manufacturing Defect

    Medtronic is recalling Distractor Rack devices used in spinal surgery due to manufacturing defects that may prevent proper device operation. Two lot numbers are affected and were distributed to facilities in Indiana, Connecticut, and Nebraska.

    Product
    Distractor Rack, REF 5598007, which may be packaged in Modular Distractor Set, Loaner Kit Number SPS03139; for use in spinal surgery
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1484-2023·2023-05-17

    ANGIOGUARD RX/XP Emboli Capture Guidewire System Separation Risk

    Cordis has recalled 684 units of ANGIOGUARD RX/XP Emboli Capture Guidewire System due to potential separation of the delivery system and capture sheath during use, which could cause stroke or require unplanned surgical intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RMC
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0872-2023·2023-05-17

    Mini Pound Cake Recalled for Undeclared Coconut Allergen

    Saint Lavian mini pound cake chocolate is being recalled because coconut is not listed on the ingredients label. Consumers with coconut allergies are at risk.

    Product
    Saint Lavian mini pound cake chocolate 2 pieces UPC: 4973341408841
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0882-2023·2023-05-17

    Smoked Wahoo Dip Recalled Due to Undeclared Yellow #5 Allergen

    Borris Brothers is recalling Smoked Wahoo Dip due to undeclared Yellow #5 (tartrazine), an allergen that may affect consumers with sensitivity. The recall affects 112 containers distributed in Florida.

    Product
    Smoked Wahoo Dip, Net Wt. 8oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1569-2023·2023-05-17

    Aesculap Caiman Articulating Surgical Device Recalled for Loose Spring

    Aesculap Caiman Articulating electrosurgical devices are being recalled because a spring may become loose and fall out during surgery, potentially entering the patient's body.

    Product
    Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery. Product Code: PL771SU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0866-2023·2023-05-17

    Sardine snack product recall for incorrect allergen labeling

    DAISO CALIFORNIA WAREHOUSE is recalling Okabe Funagata grilled sardine 43g due to incorrect allergen warning information on the package label.

    Product
    Okabe Funagata small grilled small sardine 43g UPC: 4971455077236
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0846-2023·2023-05-17

    Coffee Bonbon with Undeclared Soy, Milk, and Tree Nut Allergens Recalled

    Windy Hill Chocolate LLC is recalling Coffee Bonbon products due to undeclared allergens including soy, milk, and tree nuts. These allergens are not declared on the product label, posing a risk to consumers with allergies.

    Product
    Coffee Bonbon
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0875-2023·2023-05-17

    Kajitani Food Cigar Fry Recalled for Unlabeled Coconut

    Kajitani food cigar fry (110g, UPC 4901332108289) contains coconut that is not declared on the label. The undeclared allergen poses a health risk to consumers with coconut allergies.

    Product
    Kajitani food cigar fry 110g UPC: 4901332108289
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0843-2023·2023-05-17

    Bourbon Truffle recalled for undeclared soy, milk, tree nut allergens

    Windy Hill Chocolate LLC is recalling Bourbon Truffle candies due to undeclared allergens: soy, milk, and tree nuts. Consumers with allergies to these ingredients should not consume the product.

    Product
    Bourbon Truffle
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0883-2023·2023-05-17

    Smoked Swordfish Dip Recalled for Undeclared Yellow #5 Color Additive

    Borris Brothers voluntarily recalls 55 containers of Smoked Swordfish Dip (8oz) distributed in Florida due to undeclared Yellow #5, a color additive that can trigger reactions in sensitive individuals.

    Product
    Smoked Swordfish Dip, Net Wt. 8oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1564-2023·2023-05-17

    Bard Mission Biopsy Instrument Kit cannula and needle incompatibility

    Bard Mission Disposable Biopsy Instrument Kit has an incompatibility defect where the cannula is oversized relative to the needle, preventing proper insertion and tissue access. This could cause procedure delays and insufficient tissue collection.

    Product
    Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2023·2023-05-17

    M-Close Kit suturing apparatus recalled due to plastic housing fracture risk

    New Wave Endo-Surgical is recalling the M-Close Kit surgical suturing apparatus because the plastic housing may fracture. The recall affects 295 units distributed in Florida, Massachusetts, and Georgia.

    Product
    M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2023·2023-05-17

    APLS IgM Diagnostic Reagent Packs Recalled Due to Incorrect Conjugate

    Bio-Rad Laboratories is recalling 932 BioPlex 2200 APLS IgM Reagent Packs (Lot 301538) nationwide because they were packaged with incorrect conjugate. This could result in false-positive and false-negative test results.

    Product
    BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1576-2023·2023-05-17

    STA Compact Analyzer Firmware Bug Causes Inaccurate Test Results

    Diagnostica Stago is recalling STA Compact Analyzers due to a firmware bug causing intermittent shortened coagulation times and increased technical errors. No illnesses or injuries have been reported.

    Product
    STA Compact Automated Multi-Parametric Analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1577-2023·2023-05-17

    STA Compact Max analyzer firmware bug causes inaccurate test results

    A firmware bug in Diagnostica Stago's STA Compact Max analyzer causes intermittent shortened coagulation times and frequent technical errors that produce inaccurate lab test results. Five units were distributed to clinical laboratories nationwide.

    Product
    STA Compact Max fully automatic clinical analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0868-2023·2023-05-17

    Daisho Kimchi Hotpot Soup Recalled for Incomplete Allergen Labeling

    Daisho Kimchi hotpot soup is recalled due to incomplete allergen labeling. The label warns for fish but does not specify anchovy or sardine, and the Canadian product lists clams in ingredients but not in the allergen statement.

    Product
    Daisho Kimchi hotpot soup 750g UPC: 4904621042653
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0568-2023·2023-05-17

    Calcitonin Salmon Nasal Spray Recalled for Glass Particle Defect

    Apotex Corp. recalls Calcitonin Salmon nasal spray (82,375 bottles) nationwide due to a glass splinter entrapped in the pump mechanism. The defect renders the nasal spray inoperable.

    Product
    CALCITONIN SALMON — CALCITONIN SALMON (CALCITONIN SALMON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0570-2023·2023-05-17

    Gabapentin tablets recalled due to product mixup with foreign tablet

    The Harvard Drug Group recalled 3,984 cartons of Gabapentin 600 mg tablets distributed nationwide due to a product mixup where one foreign tablet was found.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0881-2023·2023-05-17

    Food recall: Smoked Mahi Dip undeclared Yellow #5 additive

    Borris Brothers voluntarily recalled Smoked Mahi Dip (8oz and 48oz) in Florida due to undeclared Yellow #5 food dye. Consumers sensitive to this color additive should not consume the product.

    Product
    Smoked Mahi Dip, Net Wt. 8oz and 48oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0870-2023·2023-05-17

    Wadakan Sukiyaki Sauce Recalled Due to Incomplete Fish Species Labeling

    Daiso California Warehouse is recalling Wadakan sukiyaki sauce due to incomplete allergen labeling. The product lists fish in the ingredients and contains statement but does not specify the fish species.

    Product
    Wadakan sukiyaki sauce 300ml UPC: 4903636311594
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0862-2023·2023-05-17

    Takuma food dashi salt peanut recalled for incorrect fish ingredient

    Takuma food dashi salt peanut 80g is being recalled because the product contains flying fish instead of angler fish. Consumers who purchased this product should stop using it.

    Product
    Takuma food dashi salt peanut 80g UPC: 4962679652750
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0869-2023·2023-05-17

    Ribbon raw thigh candy recalled due to incomplete fish allergen labeling

    DAISO CALIFORNIA WAREHOUSE is recalling Ribbon raw thigh candy because fish is listed without identifying the species, creating uncertainty for consumers with fish allergies.

    Product
    Ribbon raw thigh candy 65g UPC: 4903316410630
    Category
    Food
    Distribution
    6 states
  • LowFDA (Food)·F-0864-2023·2023-05-17

    Nitto Foods Immediately Pickled Dashi Recalled for Fish Labeling Issue

    Nitto Foods Immediately Pickled Dashi (5.5g x 2 bags, UPC 4902362032100) is being recalled due to labeling inconsistencies related to fish ingredients. The product was distributed across multiple US states and British Columbia.

    Product
    Nitto Foods Immediately Pickled Dashi 5.5g x 2 Bags UPC: 4902362032100
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·23V347000·2023-05-16

    2020-2022 Porsche Taycan Brake Warning Indicator Defect Recall

    Porsche is recalling 2020-2022 Taycan vehicles because the brake pad wear warning indicator displays an incorrect color, potentially causing drivers to misinterpret the warning and drive on worn brake pads with reduced braking performance.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V348000·2023-05-16

    Western Star 57X Recalled for Turn Signal Software Defect

    Daimler Trucks North America is recalling 2023 Western Star 57X vehicles because interior turn signals may flash too quickly, potentially masking burnt-out exterior bulbs and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 57X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V346000·2023-05-16

    Dennis Eagle Recalls 2020-2023 ProView Vehicles for Short Seat Belts

    Dennis Eagle is recalling 2020-2023 ProView vehicles because the driver's seat belt is too short and difficult to buckle, increasing injury risk.

    Product
    DENNIS EAGLE — DENNIS EAGLE PROVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide

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