The Recall Desk

Hazard

Class Ii recalls

1,428 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,428
Critical
0
Severe
0
Most recent
2026-07-08

Of the 1,428 class ii recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all class ii recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

376–400 of 1428

  • ModerateFDA (Devices)·Z-2283-2026·2026-06-10

    HiRes Ultra 3D cochlear implants carry an incorrect expiration date

    HiRes Ultra 3D CI HiFocus Mid Scala cochlear implants are being recalled due to an incorrect shelf-life expiration date. 36 units are affected.

    Product
    Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number: CI-1601-04 Software Version: N/A Product Description: The HiResolution Bionic Ear System is a cochlear implant designed to provide useful hearing to individuals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2269-2026·2026-06-10

    B. Braun Shands kits contain Mastisol adhesive with cracking tubing

    B. Braun CESK Shands Jacksonville kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK SHANDS JACKSONVILLE 20055717 Model/Catalog Number: 555884 Software Version: N/A Product Description: CESK SHANDS JACKSONVILLE 20055717 Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2261-2026·2026-06-10

    Shiley tracheostomy tubes recalled over incorrect display box labeling

    Covidien Shiley Tracheostomy Tubes with inner cannula, REF 6FEN, are being recalled following a customer complaint about incorrect display box labeling. 1,002 units are affected.

    Product
    COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028 The devices are intended for use in providing tracheal access for airway management. Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable inner cannulae
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2264-2026·2026-06-10

    B. Braun BlockJocks trays contain Mastisol adhesive with cracking tubing

    B. Braun BlockJocks Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable. 210 units are affected.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK, BLOCKJOCKS TRAY Model/Catalog Number: 570246 Software Version: N/A Product Description: BPSK, BLOCKJOCKS TRAY Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2263-2026·2026-06-10

    B. Braun Northside anesthesia trays contain Mastisol with cracking tubing

    B. Braun CESK Northside Anesthesia Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.

    Product
    Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2271-2026·2026-06-10

    Covidien esophageal stethoscope temperature sensors lack FDA clearance

    Covidien Mon-a-Therm Esophageal Stethoscopes with Temperature Sensor 400TM, REF 90042, are being recalled because the devices lack FDA clearance. 23,000 units are affected.

    Product
    Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0599-2026·2026-06-10

    Xyvona 3 mg levorphanol tablets recalled after proprietary name denial

    Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.

    Product
    Xyvona (levorphanol tartrate tablets), 3mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-058-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0598-2026·2026-06-10

    Xyvona levorphanol tablets recalled after FDA denied the proprietary name

    Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.

    Product
    Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV 89113, NDC 72245-762-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2270-2026·2026-06-10

    B. Braun UPMC double catheter trays contain Mastisol with cracking tubing

    B. Braun SESK UPMC Double Catheter Trays are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering it unusable.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: SESK UPMC DOUBLE CATHETER TRAY Model/Catalog Number: 530134 Software Version: N/A Product Description: SESK UPMC DOUBLE CATHETER TRAY Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2265-2026·2026-06-10

    B. Braun spinal epidural catheters contain Mastisol with cracking tubing

    B. Braun NES1725KFXL spinal epidural closed tip catheters are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack. 1,730 units affected.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH Model/Catalog Number: 530201 Software Version: N/A Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CATH Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2266-2026·2026-06-10

    B. Braun Harris Methodist kits contain Mastisol with cracking tubing

    B. Braun CESK Harris Methodist kits are being recalled because they contain Mastisol Liquid Adhesive whose butyrate tubing may crack, rendering the product unusable.

    Product
    Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2273-2026·2026-06-10

    Covidien 9 Fr Mon-a-Therm temperature probes lack FDA clearance

    Covidien Mon-a-Therm general purpose temperature probes in size 9 Fr, REF 90050, are being recalled because the devices lack FDA clearance. 128,900 units are affected.

    Product
    Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0901-2026·2026-06-10

    My Wife's Slaw made without an approved food establishment inspection

    My Wife's Slaw is being recalled because it was manufactured and distributed without the benefit of an approved food establishment inspection, so safety parameters could not be verified.

    Product
    My Wife's Slaw, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, MyWifeslaw.web.app, Zanesville, Ohio. Ingredients: Cabbage, Sugar, Vinegar, Mustard, Carrots, Onion, Bell Pepper, Salt, Black Pepper, Cayenne Pepper.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·H-0902-2026·2026-06-10

    My Wife's Slaw Jalapeno Heat made without approved facility inspection

    My Wife's Slaw Jalapeno Heat is being recalled because it was manufactured and distributed without the benefit of an approved food establishment inspection.

    Product
    My Wife's Slaw Jalapeno Heat, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, MyWifeslaw.web.app, Zanesville, Ohio. Ingredients: Cabbage, Sugar, Vinegar, Mustard, Carrots, Onion, Bell Pepper, Salt, Black Pepper, Cayenne Pepper, Jalapenos, Red Pepper Flakes.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·H-0854-2026·2026-06-03

    Fly By Jing creamy sesame noodles may contain undeclared peanut

    Fly By Jing Creamy Sesame Noodles are being recalled because possible cross-contamination resulted in an undeclared peanut allergen. 3,419 cases are affected.

    Product
    Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4 pack UPC: 8-50052-23991-6
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2259-2026·2026-06-03

    Philips Allura system hard drives may degrade and lose imaging

    Philips Allura Xper interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2242-2026·2026-06-03

    GE CARESCAPE v5 telemetry servers may lose patient monitoring signal

    GE HealthCare is recalling CARESCAPE Telemetry Server V5 ATO models because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2230-2026·2026-06-03

    Halyard nitrile exam gloves failed chemical permeation performance specifications

    Halyard Purezero Ultraviolet Nitrile Exam Gloves are being recalled because they failed to meet specifications for chemical permeation performance. 452,500 units are affected.

    Product
    Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2260-2026·2026-06-03

    Medline eye trays contain insulin syringes labeled as tuberculin syringes

    Medline EYE TRAY-LF kits are being recalled because they contain Cardinal Health syringes packaged as 1 mL tuberculin syringes but which are actually U-100 insulin syringes.

    Product
    Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2258-2026·2026-06-03

    Philips Azurion system hard drives may degrade and lose imaging

    Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2244-2026·2026-06-03

    GE CARESCAPE IOU assembly may lose ECG and SpO2 monitoring

    GE HealthCare IOU assemblies for the ARK2250 CARESCAPE Telemetry Server are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of monitoring.

    Product
    GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2243-2026·2026-06-03

    GE ApexPro disaster recovery USB kits may lose patient monitoring

    GE HealthCare ApexPro v5.0 Software Disaster Recovery USB Kits are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2245-2026·2026-06-03

    GE CARESCAPE ARK-2250L telemetry servers may lose patient monitoring

    GE HealthCare CARESCAPE Telemetry Servers ARK-2250L are being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2247-2026·2026-06-03

    GE ApexPro v6.0 software may lose ECG and SpO2 monitoring

    GE HealthCare ApexPro v6.0 eDelivery Software is being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2239-2026·2026-06-03

    HydroMARK breast biopsy markers may carry the wrong inner labeling

    HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.

    Product
    HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
    Category
    Medical Device
    Distribution
    Distributed nationwide