The Recall Desk

Archive

April 2026 recalls

694 recalls were announced in April 2026.

What the numbers show

Critical
2
Severe
134
High
430
Moderate
110
Low
18

Of the 694 recalls this month scored against our rubric, 0% are Critical, 19% are Severe.

Which agencies issued them

301–400 of 694

  • SevereFDA (Devices)·Z-1726-2026·2026-04-15

    Medline angiography and neuro kits recalled over syringe adaptor disconnection

    Medline is recalling Angio Pack and Neuro Interventional Radiology convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ANGIO PACK, Medline SKU # DYNJ57032D; 2. NEURO INTERVENTIONAL RADIOLOGY, Medline SKU # DYNJ64026C; 3. NEURO INERVENTIONAL RADI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1718-2026·2026-04-15

    NAMIC angiographic syringes recalled in the largest rotating adaptor action

    Medline is recalling NAMIC Angiographic Syringes across multiple sizes because the rotating adaptor can unwind during use and disconnect from the manifold. 1,752,096 units are affected.

    Product
    NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRING
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1729-2026·2026-04-15

    Medline TAVR procedure packs recalled over syringe adaptor disconnection risk

    Medline is recalling TAVR PACK convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 108 units are affected.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: TAVR PACK, Medline SKU # DYNJ84472
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1716-2026·2026-04-15

    Medline cath lab packs recalled over syringe rotating adaptor disconnection

    Medline is recalling cath lab and angiography procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 17,902 kits are affected.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CATH LAB PACK-LF, Medline SKU 00-HCT055P; 2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q; 3. ANGIOGRAPHY CATH LAB,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1728-2026·2026-04-15

    Medline robotic surgery packs recalled over syringe adaptor unwinding risk

    Medline is recalling Robotic Pack and Uro/Gen Robotic Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1714-2026·2026-04-15

    Medline CVOR angiography packs recalled over syringe adaptor unwinding risk

    Medline is recalling CVOR Angiography Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 3,120 kits are affected.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1721-2026·2026-04-15

    Medline head, neck and heart cath packs recalled over syringe adaptor defect

    Medline is recalling Head and Neck CDS-LF and Heart Cath Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K; 2. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 3. HEART CATH PACK-LF, Medlin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1722-2026·2026-04-15

    Medline laparoscopic and minor procedure packs recalled over syringe adaptor defect

    Medline is recalling laparoscopic herniorrhaphy, lap and minor procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. LAPAROSCOPIC HERNIORRHAPHY DSC, Medline SKU # DYNJ63021B; 2. LAP PACK, Medline SKU # DYNJ64297B; 3. MINOR PROCEDURE PACK, Medl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1712-2026·2026-04-15

    NAMIC syringe recall reaches 2.6 million units over adaptor unwinding defect

    Medline is recalling a further tranche of NAMIC Angiographic Syringes because the rotating adaptor can unwind during use and disconnect from the manifold. 2,630,369 units are affected.

    Product
    NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1719-2026·2026-04-15

    Medline non-vascular and vein packs recalled over syringe adaptor defect

    Medline is recalling Non Vascular Pack and Vein convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1713-2026·2026-04-15

    NAMIC angiographic control syringes recalled over rotating adaptor unwinding

    Medline is recalling NAMIC Angiographic Control Syringes because the rotating adaptor can unwind during use, causing a loose connection or full disconnection from the manifold. 192,690 units are affected.

    Product
    NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1784-2026·2026-04-15

    Cook Medical bile duct exploration sets labeled with overstated expiration dates

    Cook Medical is recalling the Strange Bile Duct Stone Exploration Set because affected lots were labeled with expiration dates that exceed the product's true shelf life. 49 units are affected.

    Product
    COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Number C-CSRC-7.5D-40-STRANGE, Order Number G09108
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1792-2026·2026-04-15

    Cook Medical pneumothorax tray labeled with an overstated expiration date

    Cook Medical is recalling Wayne Pneumothorax Trays because affected lots were labeled with expiration dates that exceed the product's true shelf life. 318 units are affected.

    Product
    COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Par
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1777-2026·2026-04-15

    Cook Medical CTO-18 wire guides labeled with overstated expiration dates

    Cook Medical is recalling Approach CTO-18 Micro Wire Guides because affected lots were labeled with expiration dates that exceed the product's true shelf life. 75 units are affected.

    Product
    COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1786-2026·2026-04-15

    Cook Medical multipurpose drainage catheters carry overstated expiration dates

    Cook Medical is recalling a Multipurpose Drainage Catheter because affected lots were labeled with expiration dates that exceed the product's true shelf life. 20 units are affected.

    Product
    COOK MEDICAL Multipurpose Drainage Catheter: Reference Part Number ULT8.5-38-25-P-CLMS-8-RH-FS, Order Number G29775
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1774-2026·2026-04-15

    Molded Products Luer cap sets recalled after threaded sleeve detachment complaint

    Molded Products is recalling the MPC-130 See Luer Cap Set following a confirmed complaint that the threaded sleeve was not engaged and became detached. 26,900 units are affected.

    Product
    See Luer Cap Set, MPC-130, set, administration, intravascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0663-2026·2026-04-15

    Vital Nutrients Aller-C supplement recalled for undeclared allergens

    Blueroot Health, Inc. is recalling Vital Nutrients Aller-C vitamin supplements because they contain undeclared egg, soy, and hazelnut allergens, posing a risk to consumers with allergies to these ingredients.

    Product
    Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1782-2026·2026-04-15

    Cook Medical extubation set labeled with an overstated expiration date

    Cook Medical is recalling Staged Extubation Sets because affected lots were labeled with expiration dates that exceed the product's true shelf life. 95 units are affected.

    Product
    COOK MEDICAL Cook Staged Extubation Set: Reference Part Number C-CAE-14.0-83-EXTU, Order Number G24073
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0423-2026·2026-04-15

    Cipla lanreotide prefilled syringes recalled over visual inspection deficiencies

    Cipla is recalling Lanreotide Injection 120 mg/0.5 mL prefilled syringes for lack of assurance of sterility, following an FDA observation of deficiencies in visual inspection at the contract manufacturing site.

    Product
    LANREOTIDE ACETATE — LANREOTIDE ACETATE (LANREOTIDE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0441-2026·2026-04-15

    Fagron vancomycin 1.5 gram bags recalled over sterility and detaching port part

    Fagron is recalling Vancomycin HCl 1.5 grams in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2026·2026-04-15

    Cook Medical micro wire guides labeled with overstated expiration dates

    Cook Medical is recalling Approach CTO-12 Micro Wire Guides because affected lots were labeled with expiration dates that exceed the product's true shelf life. 49 units are affected.

    Product
    COOK MEDICAL Approach CTO-12 Micro Wire Guide: Reference Part Number CMW-14-190-12G, Order Number G50787; Reference Part Number CMW-14-300-12G, Order Number G50791
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0446-2026·2026-04-15

    Teva isotretinoin 40 mg capsules recalled as superpotent and subpotent

    Teva is recalling three lots of Isotretinoin Capsules, USP, 40 mg because the product was found to be superpotent and subpotent. 8,376 packages are affected.

    Product
    ISOTRETINOIN — ISOTRETINOIN (ISOTRETINOIN)
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0443-2026·2026-04-15

    Geri-Care artificial tears lubricant eye drops recalled over sterility assurance

    Preferred Pharmaceuticals is recalling six lots of Artificial Tears Lubricant Eye Drops manufactured by Geri-Care, citing lack of assurance of sterility. 720 bottles are affected.

    Product
    ARTIFICIAL TEARS — ARTIFICIAL TEARS (GLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0427-2026·2026-04-15

    Fresenius Kabi 250 mL saline freeflex bags recalled over sterility assurance

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP supplied in 250 mL freeflex bags under its own label, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0659-2026·2026-04-15

    ReadyMeals Turkey Bacon Cheddar Pretzel Sandwich with Undeclared Sesame

    F&S Fresh Foods is recalling ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich because the sandwich contains visible sesame but the label does not declare sesame, posing a risk to consumers with sesame allergies.

    Product
    ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz, UPC 8 26766 25036 3. Distributed By F&S Fresh Foods Vineland, NJ 08360. Label declares CONTAINS EGG, MILK, SOY, WHEAT.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0651-2026·2026-04-15

    Zarlengo's chocolate gelato omits soy from the contains statement

    Zarlengo's Chocolate Gelato is being recalled because soy lecithin appears in the ingredients statement but soy is not declared in the contains statement.

    Product
    Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0430-2026·2026-04-15

    Fresenius Kabi 100 mL sodium chloride bags for BD recalled over sterility

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP in 100 mL single dose freeflex bags distributed by BD, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1779-2026·2026-04-15

    Blue Rhino G2-Multi tracheostomy introducer sets carry overstated expiration dates

    Cook Medical is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets because affected lots were labeled with expiration dates that exceed the true shelf life. 916 units are affected.

    Product
    COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set: Reference Part Number C-PTIS-100-HC-G-EU, Order Number G57685; Reference Part Number C-PTIS-100-HC-G-NA, Order Number G57682; Reference Part Number C-PTIS-100-UNL-HC-G-EU, Order Number G57687; Refer
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1794-2026·2026-04-15

    MicroScan multidrug resistance test panels recalled over incorrect processing

    MicroScan Neg Multidrug Resistant MIC 1 panels are being recalled because of a manufacturing issue involving incorrect processing of the in vitro multidrug resistant test. Three boxes are affected.

    Product
    MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried Gram Negative Breakpoint Combo Panels. MicroScan panels are designed for use in determining antimicrobial agen
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0662-2026·2026-04-15

    Riverence smoked trout dip declares cream cheese but not milk

    Riverence Smoked Trout Dip is being recalled because the label declares cream cheese in the ingredients but does not declare milk. 306 cases, or 3,672 units, are affected.

    Product
    Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is shipped to consignee frozen by the case (12/7oz. units per case). Retail container UPC 7 07651 30561 3. Case item UPC #007076513057 Label declares Ingredients: Sm
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·H-0650-2026·2026-04-15

    Zarlengo's Chocolate Chocolate Chip Gelato Recalled for Undeclared Soy Allergen

    Zarlengo Italian Ice is recalling Chocolate Chocolate Chip Gelato in multiple sizes because soy lecithin is listed in the ingredients but soy is not declared in the allergen statement, posing a risk to consumers with soy allergies.

    Product
    Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminat
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0428-2026·2026-04-15

    Fresenius Kabi 500 mL saline freeflex bags recalled over sterility assurance

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP supplied in 500 mL freeflex bags under its own label, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0440-2026·2026-04-15

    Fagron vancomycin 1.25 gram bags recalled over sterility and detaching port part

    Fagron is recalling Vancomycin HCl 1.25 grams in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1785-2026·2026-04-15

    Cricothyrotomy catheter sets labeled with overstated expiration dates

    Cook Incorporated is recalling Melker Universal Cuffed Emergency Cricothyrotomy Catheter Sets because affected lots were labeled with expiration dates that exceed the true shelf life.

    Product
    Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part Number C-TCCSB-500-UNI, Order Number G32193; Reference Part Number C-TCCSB-500-UNI-01, Order Number G47665.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1791-2026·2026-04-15

    Cook Medical Wayne pneumothorax sets carry overstated expiration dates

    Cook Medical is recalling Wayne Pneumothorax Sets because affected lots were labeled with expiration dates that exceed the product's true shelf life. 104 units are affected.

    Product
    COOK MEDICAL Wayne Pneumothorax Set: Reference Part Number C-UTPT-1020-WAYNE-IMH, Order Number G56532; Reference Part Number C-UTPT-1400-WAYNE-112497-IMH, Order Number G56535.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1789-2026·2026-04-15

    Cook Medical Spectrum central venous trays carry overstated expiration dates

    Cook Medical is recalling Spectrum Central Venous Trays because affected lots were labeled with expiration dates that exceed the product's true shelf life. 2,348 units are affected.

    Product
    COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number C-UQLMYJ-1001J-RSC-ABRM-HC-FST-A-RD, Order Number G44800; Reference Part Number C-UTLMYJ-701J-ABRM-HC-IHI-FST-A-RD, Order Number G44809; Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-FST-A-RD, Order Number G
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0438-2026·2026-04-15

    Fagron norepinephrine infusion bags recalled over sterility and detaching port part

    Fagron is recalling norepinephrine bitartrate 16 mg in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0439-2026·2026-04-15

    Fagron norepinephrine 32 mg bags recalled over sterility and port part

    Fagron is recalling norepinephrine bitartrate 32 mg in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1778-2026·2026-04-15

    Cook Medical arterial pressure monitoring trays carry overstated expiration dates

    Cook Medical is recalling Arterial Pressure Monitoring Trays because affected lots were labeled with expiration dates that exceed the product's true shelf life. 20 units are affected.

    Product
    COOK MEDICAL Arterial Pressure Monitoring Tray, Reference Part Number APMY-2.5-15-0-2.5 , Order Number G58412; Reference Part Number APMY-4.0-21J-1-12, Order Number G58419
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1804-2026·2026-04-15

    Stryker tourniquet cuffs may detach from the bladder welding connection

    Stryker Sustainability Solutions is recalling Color Cuff tourniquet cuffs because the cuff can detach from the bladder at the welding connection, leaving it unable to maintain pressure.

    Product
    Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker Sustainability Solution Color Cuff 18" (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135 Stryker Sustainability Solution Color Cuff 18" (Red)
    Category
    Medical Device
    Distribution
    41 states
  • HighFDA (Devices)·Z-1769-2026·2026-04-15

    Tornier shoulder system parts mislabeled as compatible with the HRS Max

    Tornier HRS Max tuberosity bodies and a trial component were incorrectly labeled as HRS Max products; they are compatible only with the Tornier HRS system. 233 units are affected.

    Product
    Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max Tuberosity Body No Coat, Small, Cat. No. ARS1041102 3. TORNIER HRS Max Trial, Cat. No. ARS10252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0422-2026·2026-04-15

    Cipla lanreotide syringes with safety needle recalled over sterility assurance

    Cipla is recalling Lanreotide Injection 120 mg/0.5 mL prefilled syringes supplied with a safety needle, citing lack of assurance of sterility. 54,583 syringes are affected.

    Product
    LANREOTIDE ACETATE — LANREOTIDE ACETATE (LANREOTIDE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0426-2026·2026-04-15

    Fresenius Kabi 100 mL sodium chloride freeflex bags recalled over sterility

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP supplied in 100 mL freeflex bags under its own label, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1780-2026·2026-04-15

    Blue Rhino G2-Multi tracheostomy introducer trays carry overstated expiration dates

    Cook Medical is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because affected lots were labeled with expiration dates that exceed the true shelf life. 441 units are affected.

    Product
    COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703; Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Number G57706; Reference Part Number C-PTISY-100-UNS-HC-G-NA, Order Number G57704
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1795-2026·2026-04-15

    Preeclampsia growth factor assay recalled over out-of-range quality control values

    B.R.A.H.M.S PlGF Plus KRYPTOR in vitro diagnostic tests are being recalled after customers observed out-of-range values at the lowest quality control level, which can contribute to falsely elevated results.

    Product
    B¿R¿A¿H¿M¿S KRYPTOR compact REACT, REF: 89986, used with B¿R¿A¿H¿M¿S PlGF Plus KRYPTOR, REF: 859075N, and run on the B¿R¿A¿H¿M¿S KRYPTOR compact PLUS analyzers. in vitro diagnostic test for Placental Growth Factor
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Drugs)·D-0442-2026·2026-04-15

    Fagron vancomycin infusion bags recalled over sterility and detaching port part

    Fagron Sterile Services is recalling Vancomycin HCl 1 gram in 250 mL sodium chloride bags for lack of assurance of sterility and because a blue break-off part could detach from the administration port.

    Product
    Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1773-2026·2026-04-15

    Xtant pedicle screws mislabeled with an incorrect shorter screw length

    Xtant Medical is recalling Xpress Pedicle Screw System dual lead screws from one lot that were mislabeled with a part number identifying them as shorter than they physically are.

    Product
    XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1781-2026·2026-04-15

    Cook Medical tracheostomy introducer sets labeled with overstated expiration dates

    Cook Medical is recalling Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Sets because affected lots were labeled with expiration dates that exceed the true shelf life. 484 units are affected.

    Product
    COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Reference Part Number C-PTIS-100-FLEX-HC, Order Number G32092; Reference Part Number C-PTIS-100-HC, Order Number G12115.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1790-2026·2026-04-15

    Cook Medical chest tube tray labeled with an overstated expiration date

    Cook Medical is recalling Thal-Quick Chest Tube Trays because affected lots were labeled with expiration dates that exceed the product's true shelf life. Two units are affected.

    Product
    COOK MEDICAL Thal-Quick Chest Tube Tray: Reference Part Number C-TQTSY-3200, Order Number G07242
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0433-2026·2026-04-15

    Fresenius sodium chloride 1,000 mL dialysis-supplied bags recalled over sterility

    Fresenius Kabi is recalling 0.9% Sodium Chloride Injection, USP in 1,000 mL single dose freeflex bags distributed by Fresenius Medical Care RTG, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1788-2026·2026-04-15

    Cook Medical central venous catheter sets labeled with overstated expiration dates

    Cook Medical is recalling Spectrum Central Venous Catheter Sets because affected lots were labeled with expiration dates that exceed the product's true shelf life. 5,080 units are affected.

    Product
    COOK MEDICAL Spectrum¿ Central Venous Catheter Set: Reference Part Number C-UDLM-401J-ABRM-HC, Order Number G43983; Reference Part Number C-UDLM-401J-ABRM-HC-CAH, Order Number G24754; Reference Part Number C-UDLM-401J-LSC-ABRM-HC, Order Number G43986; Reference Part Number
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1787-2026·2026-04-15

    Cook Medical nitinol stone extractors labeled with overstated expiration dates

    Cook Medical is recalling NCompass Nitinol Stone Extractors because affected lots were labeled with expiration dates that exceed the product's true shelf life. 70 units are affected.

    Product
    COOK MEDICAL NCompass¿ Nitinol Stone Extractor: Reference Part Number C-NTSE-2.4-115-NC3, Order Number G36250; Reference Part Number C-NTSE-2.4-115-NCT4, Order Number G36251.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0445-2026·2026-04-15

    Teva isotretinoin 30 mg capsules recalled as superpotent and subpotent

    Teva is recalling three lots of Isotretinoin Capsules, USP, 30 mg because the product was found to be superpotent and subpotent. 21,984 packages are affected.

    Product
    ISOTRETINOIN — ISOTRETINOIN (ISOTRETINOIN)
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0434-2026·2026-04-15

    Fresenius Kabi 1,000 mL sodium chloride bags recalled over sterility assurance

    Fresenius Kabi is recalling one batch of 0.9% Sodium Chloride Injection, USP in 1,000 mL single dose freeflex bags distributed by BD, citing lack of assurance of sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0652-2026·2026-04-15

    Zarlengo's Double Dark Chocolate Gelato recalled for undeclared soy allergen

    Zarlengo Italian Ice is recalling Zarlengo's Double Dark Chocolate Gelato in 1-gallon buckets because soy lecithin is listed in the ingredients but soy is not disclosed in the allergen statement, posing a risk to consumers with soy allergies.

    Product
    Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1783-2026·2026-04-15

    Cook Medical Spectrum central venous catheter trays carry overstated expiration dates

    Cook Medical is recalling custom Spectrum Central Venous Catheter Trays because affected lots were labeled with expiration dates that exceed the true shelf life. 1,872 units are affected.

    Product
    COOK MEDICAL Cook¿ Spectrum¿ Central Venous Catheter Tray: Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0003, Order Number G56424; Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0018, Order Number G21053; Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0042, Order Number G3
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1793-2026·2026-04-15

    Multi-parameter command modules may produce inaccurate cardiac output readings

    A circuit board issue in Multi-parameter Command Module model 91496 can start cardiac output measurement early in Auto mode, producing errors and inaccurate readings. 1,790 units are affected.

    Product
    Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0657-2026·2026-04-15

    Dadi Nongfu dried salt chilli vegetables contain the banned sweetener cyclamates

    Dadi Nongfu Dried Salt Chilli Vegetables are being recalled because the product contains cyclamates, a sweetener not permitted in food in the United States.

    Product
    DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybean oil, edible vinegar, white granulated sugar, spices, food additives (sodium glutamate, citric acid, sodium benzoate, potassium sorbate, sodium saccharin, aces
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0474-2026·2026-04-15

    Teva clonidine 0.3 mg patches recalled over unapproved raw material use

    Teva is recalling three lots of Clonidine Transdermal System, USP, 0.3 mg/day, citing CGMP deviations involving the use of an unapproved raw material. 113,943 cartons are affected.

    Product
    CLONIDINE TRANSDERMAL SYSTEM — CLONIDINE TRANSDERMAL SYSTEM (CLONIDINE)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1775-2026·2026-04-15

    Cook Medical Micro Wire Guides Recalled Due to Incorrect Expiration Dates

    Cook Incorporated is recalling specific lots of COOK MEDICAL Approach CTO-6 Micro Wire Guides because they were labeled with expiration dates that exceed their actual shelf life.

    Product
    COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6G, Order Number G50786
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1653-2026·2026-04-15

    Siemens ARTIS imaging systems may display an inflated patient dose reading

    Siemens ARTIS pheno and ARTIS Icono systems may sporadically display a major increase in the x-ray dose applied, although the actual dose applied remains within system settings and regulatory limits.

    Product
    ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0473-2026·2026-04-15

    Teva clonidine 0.2 mg patches recalled over unapproved raw material use

    Teva is recalling two lots of Clonidine Transdermal System, USP, 0.2 mg/day, citing CGMP deviations involving the use of an unapproved raw material. 62,136 cartons are affected.

    Product
    CLONIDINE TRANSDERMAL SYSTEM — CLONIDINE TRANSDERMAL SYSTEM (CLONIDINE)
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Food)·H-0658-2026·2026-04-15

    Olive skewers recalled for containing the banned sweetener cyclamates

    Olive Skewers imported by MEI YU CHENG DA TRADING are being recalled because the product contains cyclamates, a sweetener not permitted in food in the United States.

    Product
    Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar, monosodium glutamate, licorice, cloves, food additives (citric acid, DL malic acid, saccharin, sodium saccharin, steviol glycosides, aspartame, vanillin, ethy
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0472-2026·2026-04-15

    Teva clonidine transdermal patches recalled over unapproved raw material use

    Teva is recalling two lots of Clonidine Transdermal System, USP, 0.1 mg/day, citing CGMP deviations involving the use of an unapproved raw material. 124,054 cartons are affected.

    Product
    CLONIDINE TRANSDERMAL SYSTEM — CLONIDINE TRANSDERMAL SYSTEM (CLONIDINE)
    Category
    Drug
    Distribution
    0 states
  • SevereNHTSA·26V236000·2026-04-14

    Ford Bronco transfer case joint misalignment may wear driveline splines

    Ford is recalling certain 2021-2025 Bronco vehicles because a misaligned transmission to transfer case joint can wear the splines, potentially causing loss of drive power or rollaway.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V238000·2026-04-14

    Ford Recalls 2024-2026 Rangers for Sun Visor Wiring Fire Risk

    Ford is recalling 2024-2026 Ranger vehicles because improperly positioned sun visor or headliner wiring harnesses may cause an electrical short and fire in the A-pillar area.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V237000·2026-04-14

    Ford Recalls 2015-2017 F-150 Trucks for Transmission Software Defect

    Ford is recalling 2015-2017 F-150 vehicles because a signal loss can cause unexpected downshifting, increasing crash risk. Dealers will update software free of charge.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V235000·2026-04-14

    Ford F-59 front axle hub may be missing its spindle nut

    Ford is recalling certain 2025-2026 F-59 and F-53 vehicles because the front axle hub assembly may be missing the spindle nut and cotter pin, which can lead to wheel detachment.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V239000·2026-04-14

    2026 Ford Bronco Sport Engine Block Heater Fire Risk Recall

    Ford is recalling certain 2026 Bronco Sport vehicles with a 1.5L or 2.0L MPC engine and block heater because the heater may overheat when plugged in while parked, increasing fire risk.

    Product
    FORD — FORD BRONCO SPORT, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V234000·2026-04-13

    2025–2026 Harley-Davidson Softail motorcycles rear brake line defect

    Harley-Davidson is recalling certain 2025–2026 Softail motorcycles because the rear brake line may contact the Body Control Module, causing a brake fluid leak and loss of rear brakes. Loss of rear brakes increases crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FXBB, FXLRS, FXLRST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V232000·2026-04-10

    2022–2026 Kia Carnival vehicles recalled for fuel system leak risk

    Kia is recalling certain 2022–2026 Carnival vehicles because fuel may leak at the pipe connection between the fuel pipe and fuel rail, increasing the risk of fire.

    Product
    KIA — KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V229000·2026-04-10

    Genesis GV80 and related models fuel pipe leakage recall

    Hyundai Motor America is recalling certain Genesis GV70, G80, G90, and GV80 vehicles from 2021–2026 due to a fuel leak risk at the pipe connection between the fuel pipe and fuel rail, which increases the risk of fire.

    Product
    GENESIS — GENESIS G90, GV80, G80, GV70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E019000·2026-04-09

    Nova Bus Recalls Ricon Hidden Frame Windows for Detachment Risk

    Nova Bus is recalling Ricon hidden frame windows sold through Prevost due to inadequate adhesion that may cause glass to detach, increasing crash injury risk.

    Product
    VISIBILITY:GLASS, SIDE/REAR:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26385·2026-04-09

    BISSELL steam cleaner attachments can detach and expel hot water

    BISSELL Steam Shot OmniReach and Omni handheld steam cleaners are recalled after 206 reports of hot water or steam escaping from the attachments, including 161 reports of burn injuries.

    Product
    Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26372·2026-04-09

    Osprey robotic pool vacuum batteries can overheat and catch fire

    Osprey 700 Max and S1 robotic pool vacuums are recalled because the lithium-ion battery can overheat. Ten reports of overheating or fire have caused nine incidents of property damage; no injuries reported.

    Product
    Osprey 700 Max and S1 robotic pool vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V227000·2026-04-09

    Honda Odyssey side air bags may deploy unexpectedly from software error

    Honda is recalling certain 2018-2022 Odyssey vehicles because a software programming error can cause the side and side curtain air bags to deploy unexpectedly. 440,830 vehicles are affected.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V228000·2026-04-09

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Software Defect

    Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 school buses because a software defect may prevent warning lights and the stop sign arm from activating.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V226000·2026-04-09

    IC Bus Recalls EVSB School Buses Due to High Voltage Switch Defect

    International Motors is recalling 2022-2027 IC Bus EVSB school buses because a high voltage disconnect switch may fail to shut off power, posing a risk of electrical shock.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26393·2026-04-09

    SCUBAPRO weight pocket D-ring handles can detach during a dive

    SCUBAPRO Monorail Weight Pockets are recalled because the D-ring handle used to release the pocket from a buoyancy compensator can detach, preventing weight ditching in an emergency.

    Product
    SCUBAPRO Monorail Weight Pockets for BCDs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26395·2026-04-09

    Head ski boot shell and sole inserts can deteriorate and break

    Head ski boots with fluorescent yellow components from model years 2016 through 2022 are recalled because those materials can deteriorate and break, posing a risk of injury from a fall.

    Product
    Head Ski Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04092026-01·2026-04-09

    Beef and Pork Products Recalled for Undeclared Sesame Allergen

    Sky Ranch Meat LLC marinated beef and pork products may contain undeclared sesame allergen. The products are no longer available for purchase, but consumers who have them at home are urged not to consume them.

    Product
    Sky Ranch Meat LLC — FSIS Issues Public Health Alert for Beef and Pork Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    4 states
  • HighCPSC·26387·2026-04-09

    Easymake adult portable bed rails pose entrapment and asphyxiation hazard

    Easymake adult portable bed rails are recalled because users can become entrapped within the rail or between the rail and the mattress, posing a risk of death by asphyxiation.

    Product
    Easymake Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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