The Recall Desk

Archive

August 2026 recalls

472 recalls were announced in August 2026.

What the numbers show

Critical
55
Severe
146
High
210
Moderate
52
Low
9

Of the 472 recalls this month scored against our rubric, 12% are Critical, 31% are Severe.

Which agencies issued them

101–200 of 472

  • ModerateFDA (Devices)·Z-2950-2026·2026-08-26

    EndoFLIP System Recall Due to Incorrect Catheter Expiration Flags

    FDA is recalling 327 EndoFLIP Systems because a software error incorrectly flags catheters as expired, making them unavailable for clinical procedures.

    Product
    EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684 Endoscopic measuring system, including catheter components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0765-2026·2026-08-26

    Shilpa Medicare Recalls Discolored PEMRYDI RTU Injection Vials

    Shilpa Medicare is recalling 9,489 vials of PEMRYDI RTU (pemetrexed disodium) due to reports of green to dark green discoloration in the solution.

    Product
    PEMRYDI RTU — PEMRYDI RTU (PEMETREXED DISODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-1235-2026·2026-08-26

    Prospector Popcorn Recalled for Inaccurate Nutrient Labeling

    Prospector Popcorn is recalling Belgian Chocolate Toffee Gourmet Popcorn due to inaccurate nutrient declarations for Iron and Vitamin D.

    Product
    Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz
    Category
    Food
    Distribution
    45 states
  • LowFDA (Devices)·Z-2972-2026·2026-08-26

    Paragon 28 Recalls Custom Foot Implant Due to Material Defect

    Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.

    Product
    Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; foot implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V550000·2026-08-25

    Ford Recalls 2026 Maverick, F-150, and Bronco Sport for Joint Issues

    Ford is recalling 2026 Maverick, F-150, and Bronco Sport vehicles because improperly tightened joints may lead to detached parts or loss of vehicle control.

    Product
    FORD — FORD MAVERICK, F-150, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V548000·2026-08-25

    Ford Recalls 2026 Vehicles for Engine Piston Dome Manufacturing Defect

    Ford is recalling 2026 Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles because incorrectly manufactured engine piston domes may fail, causing a loss of drive power.

    Product
    FORD — FORD EXPLORER, BRONCO SPORT, BRONCO, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V547000·2026-08-25

    Ford Recalls 2024-2026 Mustangs for Wiring Harness Ground Fracture Risk

    Ford is recalling 2024-2026 Mustangs because engine compartment wiring harness ground connections may fracture, potentially causing loss of drive power or essential vehicle functions.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V549000·2026-08-25

    Mitsubishi Recalls Outlander Models for Rearview Camera Software Defect

    Mitsubishi is recalling 2025-2026 Outlander and 2026 Outlander PHEV vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER PHEV, OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V546000·2026-08-24

    2027 Thomas Built School Buses Recalled for Missing Seat Belt Anchor Plates

    Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER EFX2 and HDX2 school buses because missing connector plates may compromise seat belt anchorages and body joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX2, SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E060000·2026-08-24

    Rennline Recalls Lower Control Arms Due to Subframe Damage Risk

    Rennline Automotive is recalling 106 lower control arms that may have incorrect dimensions, potentially damaging the subframe and causing loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V542000·2026-08-21

    T.A. Pelsue Recalls 2024-2025 Trailers Due to Axle Bracket Defect

    T.A. Pelsue is recalling 2024-2025 Fost XL, FiberLite, and MPCCT trailers because axle mounting brackets may crack and fail, increasing crash risk.

    Product
    PELSUE — PELSUE MPCCT, FOST XL, FIBERLITE XL TRADESMAN, FIBERLITE POD TRADESMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V544000·2026-08-21

    PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Seat Heater Fire Risk

    PACCAR is recalling 811 specific 2027 Kenworth and Peterbilt trucks because a missing heat-shrink on the seat ventilation harness may cause a short circuit and fire.

    Product
    PETERBILT — PETERBILT, KENWORTH 589, W990, T880, T680
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V541000·2026-08-21

    Altec Recalls Aerial Devices and Digger Derricks Due to Braking Calibration Issue

    Altec is recalling specific aerial devices and digger derricks because the automatic braking system was not recalibrated after moving the front radar box, increasing crash risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AM SERIES AERIAL DEVICE, AA SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V538000·2026-08-20

    Rossmonster Recalls 2026 Motorcoaches Due to Rooftop Fan Fire Risk

    Rossmonster is recalling 2026 Baja, Skye, and Havn motorcoaches because a rooftop ventilation fan component may overheat and cause a fire.

    Product
    ROSSMONSTER — ROSSMONSTER BAJA, SKYE, HAVN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V540000·2026-08-20

    Lucid Recalls 2022-2026 Air Vehicles Due to Fire Risk

    Lucid is recalling 2022-2026 Air vehicles because an electrical circuit may overheat, increasing the risk of fire or reduced visibility.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26710·2026-08-20

    KTM Recalls GASGAS and Husqvarna Off-Road Motorcycles Due to Brake Defect

    KTM North America is recalling approximately 21,040 GASGAS and Husqvarna off-road motorcycles because the rear brake caliper can crack or break, posing a crash risk.

    Product
    GASGAS and Husqvarna Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26711·2026-08-20

    Modine Recalls Airedale Ventilation Fans in School Heat Pumps Due to Fire Hazard

    Modine is recalling Airedale ventilation fans in specific school heat pumps because water exposure can cause short circuits and fires. No injuries have been reported.

    Product
    Ventilation Fans in ClassMate® DX Cooling and Air Source Heat Pumps and SchoolMate® Water/Ground Source Heat Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26713·2026-08-20

    JINHEZO LED Tea Lights Recalled for Battery Ingestion Risk

    CPSC recalls JINHEZO Mini Waterproof LED Tea Lights because accessible button batteries pose a serious injury or death risk if swallowed.

    Product
    JINHEZO Mini Waterproof LED Tea Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26712·2026-08-20

    Goal Zero Recalls YETI 3000X Power Stations for Fire and Burn Hazards

    Goal Zero is recalling about 46,200 YETI 3000X portable power stations because the circuit board can overheat, posing a risk of fire and burn injuries.

    Product
    Goal Zero YETI 3000X Portable Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V568000·2026-08-20

    Ford F-650 SD Recall: Liftgate Platform Deck Pins May Break

    Marathon Industries is recalling one 2025 Ford F-650 SD because deck pins may break, causing the liftgate platform to fall and increasing injury risk.

    Product
    FORD — FORD F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C006000·2026-08-20

    Britax Recalls Infant Car Seats Due to Handle Detachment Risk

    Britax is recalling specific infant car seats because a screw in the carrying handle may come loose, causing the handle to partially detach and increasing the risk of a child falling.

    Product
    CHILD SEAT:CRITICAL FASTENERS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26716·2026-08-20

    CCM Hockey Recalls FMHVR Visors and ACCHVR Accessories Due to Laceration Risk

    CCM Hockey is recalling FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories because they can crack upon impact, posing a risk of laceration or impact injury.

    Product
    FMHVR Hybrid Visors and ACCHVR Replacement Visor Accessories
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26714·2026-08-20

    Koorlian Mattresses Recalled for Fire Hazard Violating Flammability Standards

    CPSC recalls Koorlian mattresses sold on Amazon due to fire risks from violating mandatory flammability standards. Consumers should stop using them and contact the manufacturer for a free cover.

    Product
    Koorlian Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V539000·2026-08-20

    GM Recalls Buick and Chevrolet SUVs for Rearview Camera Defect

    General Motors is recalling 2024-2026 Buick and Chevrolet SUVs because the rearview camera may display a distorted or blank image, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAX, TRAILBLAZER, ENVISTA, ENCORE GX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1293-2026·2026-08-19

    Taylor Farms Recalls Markon Lettuce Salad Mix for Potential Cyclospora

    Taylor Farms is recalling Markon Lettuce Salad Mix products due to potential Cyclospora contamination. The recall affects 1,575 cases distributed across 28 US states and Mexico.

    Product
    MARKON LETTUCE SALAD MIX 4/5# MARKON LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1298-2026·2026-08-19

    Taylor Farms Recalls Mixed Lettuce Products Due to Cyclospora Risk

    Taylor Farms de Mexico is recalling specific lots of mixed lettuce products due to potential Cyclospora contamination. The products were distributed to 28 U.S. states and Mexico.

    Product
    MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1229-2026·2026-08-19

    Midwest Poultry Service Recalls Simple Truth Eggs for Salmonella Risk

    Midwest Poultry Service is recalling 1.59 million dozen Simple Truth and bulk eggs due to a possible Salmonella Enteritidis contamination.

    Product
    Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Truth, Natural Cage Free Grain Fed, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-87032 0. Distributed by The Kroger Co., Cincinnati, OH 45202. 2. Simple Truth, Natural Cag
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·H-1294-2026·2026-08-19

    Taylor Farms Recalls Peak Lettuce Salad Due to Cyclospora Risk

    Taylor Farms is recalling specific Peak Lettuce Salad products due to potential Cyclospora contamination. Consumers should check for specific codes and stop eating the product.

    Product
    PEAK LETTUCE SALAD W/BAG 4/5# Iceberg, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1284-2026·2026-08-19

    Taylor Farms Recalls Iceberg Lettuce Due to Potential Cyclospora Contamination

    Taylor Farms is recalling specific lots of chopped and shredded iceberg lettuce due to potential Cyclospora contamination. The products were distributed to 28 states and Mexico.

    Product
    SYSCO LETTUCE CHOP 4/5# SYSCO LETTUCE SHRED 1/8" 4/5# Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1300-2026·2026-08-19

    Piazza Produce Recalls Garden Salad Due to Possible Cyclospora Contamination

    Piazza Produce is recalling Garden Salad products due to possible Cyclospora contamination. The recall affects 1,279 units sold in six states.

    Product
    Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·H-1230-2026·2026-08-19

    Midwest Poultry Services Recalls Eggs for Possible Salmonella Enteritidis

    Midwest Poultry Services is recalling 1.59 million dozen eggs due to possible Salmonella Enteritidis contamination. The recall affects Kroger, Brookshire's, and Country Morning brands in six states.

    Product
    Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-60902 1. Distributed by The Kroger Co., Cincinnati, OH 45202. 2. Kroger, Medium, 30 Eggs, Net Wt 52.5 oz (3lb 4.5oz) 596g, UP
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·H-1290-2026·2026-08-19

    Taylor Farms Recalls Iceberg and Romaine Lettuce Blends Due to Cyclospora Risk

    Taylor Farms de Mexico is recalling specific lots of Sysco blend lettuce products due to potential Cyclospora contamination. The recall affects 1,834 cases distributed across 28 US states and Mexico.

    Product
    SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# SYSCO BLEND LETT/ROM 70/30 NOCOLR 4/5# SYSCO BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1228-2026·2026-08-19

    Bazzini Dark Chocolate Coconut Almond Bites Recalled for Undeclared Peanuts

    Bazzini LLC is recalling Dark Chocolate Coconut Almond Bites distributed in Washington due to undeclared peanuts, a major food allergen.

    Product
    Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·H-1285-2026·2026-08-19

    Taylor Farms Iceberg Lettuce Recalled for Potential Cyclospora Contamination

    Taylor Farms is recalling specific iceberg lettuce products due to potential Cyclospora contamination. The recall affects 16,314 cases distributed across 28 US states and Mexico.

    Product
    TAYLOR FARMS LETTUCE CHOP 1X1" 4/4# TAYLOR FARMS LETTUCE CHOP 1X1" 8/2# TAYLOR FARMS LETTUCE CHOP 4/5# TAYLOR FARMS LETTUCE SHRED 1/4" 4/5# TAYLOR FARMS LETTUCE SHRED 1/8" 4/5# TF LETTUCE CHOP .5X.5" 4/5 LB Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1281-2026·2026-08-19

    Taylor Farms Recalls Markon Iceberg Lettuce Due to Cyclospora Risk

    Taylor Farms is recalling specific Markon iceberg lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and stop using affected items.

    Product
    MARKON LETTUCE CHOP 4/5# MARKON LETTUCE SHRED 1/4" 4/5# MARKON LETTUCE SHRED 1/8" 4/5# MARKON LETTUCE SHRED 3/8" 4/5# Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Drugs)·D-0772-2026·2026-08-19

    Victory Medical Center Pharmacy Recalls Glutathione Vials Due to Contamination

    Victory Medical Center Pharmacy is recalling 91 vials of Glutathione (MDV) 200 mg/mL due to bacterial endotoxin contamination.

    Product
    Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0773-2026·2026-08-19

    Optiray Injection Recalled for Presence of Particulate Matter

    Liebel-Flarsheim is recalling 3,486 vials of Optiray Injection due to the presence of particulate matter, including plastic, stainless steel, and glass.

    Product
    OPTIRAY — OPTIRAY (IOVERSOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0769-2026·2026-08-19

    Buy-Herbal Recalls Kian Pee Wan Capsules for Undeclared Drug Ingredients

    Buy-Herbal is recalling Kian Pee Wan Capsules because they contain undeclared dexamethasone and cyproheptadine. The product was sold to consumers via an eBay third-party seller.

    Product
    Kian Pee Wan Capsules, 30-count bottles
    Category
    Drug
    Distribution
    0 states
  • CriticalFDA (Food)·H-1295-2026·2026-08-19

    Taylor Farms Recalls Lettuce Salad Mix for Potential Cyclospora Contamination

    Taylor Farms is recalling specific lots of Sysco lettuce salad mix due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.

    Product
    SYSCO LETTUCE SALAD MIX 4/5# SYSCO LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1296-2026·2026-08-19

    Taylor Farms Lettuce Salad Recalled for Potential Cyclospora Contamination

    Taylor Farms is recalling specific bags of lettuce salad due to potential Cyclospora contamination. The products were distributed to 28 U.S. states and Mexico.

    Product
    TAYLOR FARMS LETTUCE SALAD W/BAG 4/5# Iceberg, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1297-2026·2026-08-19

    Cross Valley Farms Lettuce Blend Recalled for Potential Cyclospora Contamination

    Taylor Farms de Mexico is recalling Cross Valley Farms lettuce blends due to potential Cyclospora contamination. The products were distributed to multiple US states and Mexico.

    Product
    Cross Valley Farms BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1292-2026·2026-08-19

    Cross Valley Farms Lettuce Salad Mix Recalled for Cyclospora Risk

    Taylor Farms is recalling Cross Valley Farms lettuce salad mix products due to potential Cyclospora contamination.

    Product
    Cross Valley Farms LETTUCE SALAD MIX 4/5# Cross Valley Farms LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1299-2026·2026-08-19

    Taylor Farms Recalls Pre-Blended Lettuce Due to Cyclospora Contamination

    Taylor Farms is recalling pre-blended lettuce products due to potential Cyclospora contamination. The recall affects 1,161 cases distributed across 28 US states and Mexico.

    Product
    TAYLOR FARMS BLEND LETT/ROM BLEND WITH BAG 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1287-2026·2026-08-19

    Taylor Farms Recalls Shredded Iceberg Lettuce Due to Cyclospora Contamination

    Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed to 28 U.S. states and Mexico.

    Product
    YUM LETTUCE SHREDDED 1/4" 6/5# Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·H-1279-2026·2026-08-19

    Cross Valley Farms Iceberg Lettuce Recalled for Potential Cyclospora Contamination

    Taylor Farms is recalling specific lots of Cross Valley Farms iceberg lettuce due to potential Cyclospora contamination. The products were distributed across 28 US states and Mexico.

    Product
    Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4" 4/5# Cross Valley Farms LETTUCE SHRED 1/8" 4/5# Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·H-1282-2026·2026-08-19

    Taylor Farms Recalls Shredded Iceberg Lettuce Due to Cyclospora Contamination

    Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed across 28 U.S. states and Mexico.

    Product
    PEAK LETTUCE SHRED 1/8" 4/5# Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0755-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2922-2026·2026-08-19

    Surgipro II Sutures Recalled for Potential Sterile Barrier Defects

    FDA is recalling Surgipro II sutures due to potential sterile packaging defects that could cause biocontamination and infection.

    Product
    Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0754-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1270-2026·2026-08-19

    529 Commerce Recalls Aquafaba Powder for Undeclared Egg

    529 Commerce, LLC is recalling Aquafaba Powder, Vegan Replacement, because it contains undeclared egg. The product was distributed to 24 states.

    Product
    Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with zipper. UPC 99284 53095 and UPC 99284 30622
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·H-1280-2026·2026-08-19

    Taylor Farms Recalls Marketside Iceberg Salad for Potential Cyclospora Contamination

    Taylor Farms is recalling specific Marketside iceberg salad products due to potential Cyclospora contamination. Consumers should check lot codes and discard affected items.

    Product
    MARKETSIDE ICEBERG SALAD 10/24 oz, UPC 681131328951; MARKETSIDE ICEBERG SALAD 12/12 oz, UPC 681131328944; MARKETSIDE SHREDDED LETT 12/16 oz, UPC 681131532099; MARKETSIDE SHREDDED LETT 12/8 oz, UPC 681131328968; Iceberg only products.
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0757-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 20mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0752-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.

    Product
    SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0749-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0753-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.

    Product
    SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0756-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 500 vials of Semaglutide 10mg due to the presence of nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0766-2026·2026-08-19

    Prestige Recalls Clear Eyes Maximum Itchy Eye Relief Due to Sterility Concerns

    Prestige Brands Holdings is recalling Clear Eyes Maximum Itchy Eye Relief eye drops due to a lack of assurance of sterility and potential contamination.

    Product
    CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0748-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1288-2026·2026-08-19

    Taylor Farms Recalls Cross Valley Farms Lettuce Due to Cyclospora Risk

    Taylor Farms is recalling specific Cross Valley Farms lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and discard or return affected items.

    Product
    Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-2873-2026·2026-08-19

    Spectra Medical Devices Recalls Sodium Chloride Injection Ampules Due to Sterility Concerns

    Spectra Medical Devices is recalling Sodium Chloride Injection ampules because manufacturing issues may have compromised sterility, posing a risk of infection or inflammation to patients.

    Product
    Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flush for IV tubing systems and indwelling intravascular access devices.
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0750-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 9,762 vials of Semaglutide 4.5mg due to the presence of nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0762-2026·2026-08-19

    Shoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations

    Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.

    Product
    TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO 171596-29-5), NDC 85702-001-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0787-2026·2026-08-19

    Baxter Recalls Cefazolin Injection Bags Due to Particulate Matter

    Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.

    Product
    CEFAZOLIN — CEFAZOLIN (CEFAZOLIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1289-2026·2026-08-19

    Taylor Farms Recalls Iceberg and Romaine Lettuce for Potential Cyclospora

    Taylor Farms de Mexico is recalling specific lots of iceberg and romaine lettuce blends due to potential Cyclospora contamination.

    Product
    MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-0747-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.

    Product
    SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1291-2026·2026-08-19

    Taylor Farms Recalls Garden Salad Mix Due to Potential Cyclospora Contamination

    Taylor Farms is recalling specific lots of garden salad mix and lettuce blends due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.

    Product
    TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# NATIONAL TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# ND TAYLOR FARMS BLEND LETT/ROM 50/50 NOCLR 4/5# TAYLOR FARMS BLEND LETT/ROM 70/30 NOCOLR 4/5# TAYLOR FARMS BLEND LETT/ROM 80/20 4/5# TAYLOR FARMS LETTUCE SALAD MIX 4/5# Iceberg
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-2938-2026·2026-08-19

    Erbe ERBECRYO 2 Cryosurgical Unit Recalled Due to Rupture Risk

    Erbe USA Inc is recalling ERBECRYO 2 Cryosurgical Units because a strong pull on the high-pressure transfer hose may cause the cryoprobe to rupture.

    Product
    ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2920-2026·2026-08-19

    Dermalon Sutures Recalled for Potential Sterile Barrier Packaging Defects

    Covidien is recalling Dermalon 4-0 sutures because sterile barrier packaging may be perforated or torn, risking biocontamination and infection.

    Product
    Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2921-2026·2026-08-19

    Surgipro Sutures Recalled for Potential Sterile Barrier Perforation

    FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.

    Product
    Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2923-2026·2026-08-19

    Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness

    Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness.

    Product
    Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count, 150 count, Product Number MSC351400AN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0751-2026·2026-08-19

    Apollo Care Recalls Semaglutide Vials Due to Particulate Matter

    Apollo Care, LLC is recalling specific lots of Semaglutide 9mg vials because they contain nylon and silk-type particulate matter.

    Product
    SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2943-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges

    Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.

    Product
    Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2947-2026·2026-08-19

    Cardinal Health Recalls Neurological Procedure Kits Due to Endotoxin Variability

    Cardinal Health is recalling specific Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.

    Product
    Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC28; 3) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC2C; 4) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2933-2026·2026-08-19

    OBP Medical Recalls Vaginal Speculums Due to Potential Sharp Edges

    OBP Medical is recalling ER-Spec Single-Use Vaginal Speculums because a burr on the plastic blade may create a sharp edge, posing a risk of injury to patients and providers.

    Product
    OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2937-2026·2026-08-19

    Bioporto ProNephro AKI Reagent Kit Recalled for Non-Validated Rework Process

    Bioporto Diagnostics is recalling ProNephro AKI Reagent Kits because a non-validated rework process could lead to missed diagnoses of renal disease.

    Product
    ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2946-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges

    Cardinal Health is recalling 602 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.

    Product
    Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY , Catalog Number: SNE30CNOHE; 3) NEURO MAJOR 2 PACK , Catalog Number: SNE30CRJGY; 4) NEURO PACK , Catalog Number: SNE43
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2934-2026·2026-08-19

    Waldemar Link Recalls Endo-Model Tibial Plateau Replacement Sets

    Waldemar Link is recalling Endo-Model tibial plateau replacement sets that incorrectly contain a Pure Hinge plateau, posing a risk of increased wear if implanted.

    Product
    Endo-Model, Replacement Set, Tibial Plateau, right/left, L, UHMWPE, CoCrMo, Rotating Hinge Item Number 15-0027/16
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2941-2026·2026-08-19

    BD Medical Extension Sets Recalled for Potential Sterilization Defects

    BD Switzerland is recalling 93,700 intravascular extension sets because they may not have received adequate sterilization processing.

    Product
    60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site REF MPX5305-C UDI-DI code: 10885403274619 9 IN Extension Set w/Max Y REF MPX5300-C UDI-DI code: 10885403237218 Intravascular Administration Set and Extens
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-2926-2026·2026-08-19

    Medline Micro-Kill Bleach Germicidal Wipes Recalled for Reduced Concentration

    Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because bleach concentration may drop below specification, potentially compromising disinfection effectiveness.

    Product
    Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2918-2026·2026-08-19

    V-Loc 90 Absorbable Wound Closure Devices Recalled for Packaging Defects

    Covidien, LP is recalling V-Loc 90 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that may cause biocontamination.

    Product
    V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12 VLOCM0003 VLOCM0013 V-LOC* 90 4-0 CLR 30CM P12X12 VLOCM0013 VLOCM0024 V-LOC* 90 3-0 CLR 45CM P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2912-2026·2026-08-19

    Microvention Recalls Bobby Balloon Guide Catheters Due to Pinhole Defects

    Microvention Inc. is recalling 5,500 Bobby Balloon Guide Catheters worldwide due to an increased rate of balloon pinhole defects.

    Product
    BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2924-2026·2026-08-19

    Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness

    Medline is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness, potentially allowing pathogenic microorganisms to survive.

    Product
    Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2925-2026·2026-08-19

    Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness

    Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.

    Product
    Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2945-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges

    Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.

    Product
    Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4) KIT, SINUS , Catalog Number: PE13SPAJC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2919-2026·2026-08-19

    V-Loc 180 Absorbable Wound Closure Device Recalled for Packaging Defects

    FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.

    Product
    V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE BOX01482V2 BOX BYPASS KIT DEZEMBER 2025 BOX09222V1 BOX BYPASS KIT NEU BOX 003
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1224-2026·2026-08-19

    SHEANDRO Vodka Tomato Sauce Recalled for Undeclared Milk Allergen

    SHEANDRO LLC is recalling Vodka Tomato Sauce because the label declares cream and cheese but fails to declare milk, a major allergen.

    Product
    Vodka Tomato Sauce, NET WT. 24 oz / 680g, glass jar packed 12 jars in a carton.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2766-2026·2026-08-19

    Baxter Duo-Vent Solution Set Recalled for Air Bubbles in Tubing

    Baxter Healthcare is recalling 24,528 units of Duo-Vent Solution Sets due to customer reports of air bubbles in the drip chamber and tubing.

    Product
    Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2931-2026·2026-08-19

    Philips Azurion Rystem X-Ray System Software Recall for Image Quality Issues

    Philips is recalling Azurion Rystem X-ray systems due to software defects that may degrade image quality or lose geometry movements, potentially delaying therapy or causing procedural complications.

    Product
    Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222,722223, 722224, 722225, 722226, 722227, 722228, 722280*, 722281*, and 722282* (*These models are distributed only in China), with Software Version Number R2.2.10 and R2.1.10*
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2932-2026·2026-08-19

    Philips Azurion Fluoroscopy System Recall for Software Image Quality Issues

    Philips is recalling 2,016 Azurion interventional fluoroscopic x-ray systems worldwide due to software defects that may degrade image quality or lose geometry movements, potentially delaying therapy or causing procedural complications.

    Product
    Philips Azurion, Model Numbers: 722229, 722230, 722231, 722232, 722233, 722234, 722235, and 722236, with Software Version Numbers: R3.0 and R3.1; Interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2936-2026·2026-08-19

    BioFire Respiratory Panel 2.1 Recalled for Increased False Negative Results

    BioFire Diagnostics is recalling 2,370 pouches of the BIOFIRE Respiratory Panel 2.1 test due to an increase in false negative results.

    Product
    BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2944-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability

    Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.

    Product
    Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2928-2026·2026-08-19

    Philips Allura Xper FD Fluoroscopic X-Ray System Recalled for Firmware Issue

    Philips is recalling 4,252 Allura Xper FD interventional fluoroscopic x-ray systems worldwide due to a firmware issue that may cause loss of geometry movements.

    Product
    Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2948-2026·2026-08-19

    Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges

    Cardinal Health 200, LLC is recalling 52,699 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.

    Product
    Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH5; 4) KIT, ANT CERVICAL DISC , Catalog Number: PN41
    Category
    Medical Device
    Distribution
    Distributed nationwide

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