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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-07-29FDA-DeviceMedtronic NeurosurgeryClass IIMedtronic Ventriculostomy Kit recalled for endotoxin contamination
Medtronic Neurosurgery's Ventriculostomy Kit (REF: 46154) may contain endotoxin levels higher than safe limits for devices that contact cerebrospinal fluid during brain surgery. Endotoxin exposure can trigger acute inflammation in the brain and nervous system.
- 2026-07-29FDA-DevicePIE Medical Imaging B.V.Class IIPIE Medical 3mensio software recalled for cardiac measurement errors
The 3mensio Workstation software may report heart and vessel measurements that are 0.8% to 34% larger than the actual size when specific conditions are met: the software is used with access only to 3D Echo or Mitral 3D Echo features, and the analysis involves Philips 3D echo datasets that contain Color Doppler data. This could lead to incorrect clinical measurements used in patient care decisions.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline procedure kits recalled for medication quality issues
Medline medical procedure kits used for knee and hip surgeries contain pain management medications with quality issues that could make them less effective. The affected kits were distributed to hospitals and surgical centers in Missouri, Colorado, and Illinois.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline HIP CDS-LF procedure kit recalled for drug ineffectiveness
Medline medical procedure convenience kits (model HIP CDS-LF) contain pain management medications with quality issues that could make the medication ineffective. The affected kits were distributed in Missouri, Colorado, and Illinois. No injuries have been reported.
- 2026-07-29FDA-DeviceAVID Medical, Inc.Class IIHalyard EYE PACK recalled for incorrect Betadine concentration
Certain Halyard EYE PACK convenience kits (Model LVEY27) contain Betadine solution at an incorrect concentration. The kits were distributed nationwide, primarily in California. No injuries have been reported.
- 2026-07-29FDA-DeviceSEASPINE ORTHOPEDICS CORPORATIONClass IISeaSpine Polyaxial Head recalled for potential intraoperative pop-off
SeaSpine Orthopedics has recalled certain Polyaxial Head spinal implants (REF 41-3010) due to a manufacturing error that may cause the polyaxial head to detach from the screw during surgery after insertion. This could require additional surgical intervention. The recall affects 796 units distributed worldwide, including nationwide US distribution and locations in Chile and Australia.
- 2026-07-29FDA-DeviceOlympus Corporation of the AmericasClass IIOlympus 4K UHD LCD Monitor recalled for connector faults
Olympus has identified a potential fault in the HDMI and DisplayPort connectors on certain OEV321UH 4K UHD LCD Monitors. This fault can result in image loss or display abnormalities. The recall affects 10 units with specific serial numbers distributed in Ohio, California, New Jersey, Florida, and Japan.
- 2026-07-29FDA-DeviceFerno-Washington IncClass IIFerno-Washington Power F2 stretcher system recalled for jamming risk
The roller assembly on the Ferno-Washington Power F2 Powered Fastening System may wear unevenly and deform, causing the rail mechanism to jam. If this happens, the stretcher cannot move along the rail—either with the powered system or manually—potentially delaying patient transport to a hospital.
- 2026-07-29FDA-DeviceICU Medical Inc.Class IIICU Medical Hotline Fluid Warming Set recalled for leakage risk
ICU Medical's Hotline Fluid Warming Set (model L-70), a single-use device used to warm blood and IV fluids before delivery to patients, may leak due to inadequate solvent application at the tubing-to-connector bond in certain production lots. This defect could affect proper fluid delivery during patient care.
- 2026-07-29FDA-DeviceParagon 28, Inc.Class IIParagon 28 guide rod recalled for sterile packaging breach
Paragon 28 received two complaints about breaches in the sterile barrier packaging of specific lots of the Phantom Hindfoot TTC/TC Ball Tipped Guide Rod (0.30 mm, 800 mm). The packaging breach could potentially allow contamination of the surgical device before use. No injuries have been reported.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE Steerable Sheath recalled for air embolism risk
Boston Scientific identified that certain FARADRIVE Steerable Sheath devices may develop damage to the hemostatic valve if the dilator is not inserted correctly during preparation. Valve damage can allow air to enter the device, which may lead to air embolism—a serious condition where air bubbles reach the bloodstream and heart.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE Steerable Sheath recalled for air embolism risk
Boston Scientific identified that certain lots of the FARADRIVE Steerable Sheath (CLEAR) may have a hemostatic valve that can be damaged during device preparation if the dilator is not inserted correctly. Valve damage can allow air to enter, potentially causing an air embolism and patient harm.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE sheath recalled for air embolism risk
Boston Scientific has identified that certain lots of the FARADRIVE steerable sheath may develop damage to the hemostatic valve during preparation if the dilator is not inserted correctly. This valve damage can allow air to enter the device, which may lead to air embolism (air in the bloodstream) and patient harm.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARADRIVE Sheath recalled for air embolism risk
Boston Scientific identified that improper dilator insertion during device setup can damage the hemostatic valve in the FARADRIVE Steerable Sheath. Valve damage may allow air to enter the device, potentially causing air embolism and patient harm. The risk occurs in a subset of affected units when the dilator is not inserted straight through the center of the valve.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARASTAR PFA Generator recalled for incompatibility
Boston Scientific identified specific FARASTAR Pulsed Field Ablation (PFA) generators with a configuration that cannot work safely with the FARAPOINT PFA catheter. Six units with specific serial numbers were distributed across Europe and need to be replaced.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARASTAR PFA Generator recalled for incomplete labeling
Boston Scientific distributed 11 FARASTAR PFA Generator devices with Instructions For Use that were missing information about the FARAPOINT PFA catheter. The incomplete labeling could affect proper device use and patient safety.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARASTAR ablation generator recalled for incomplete instructions
Boston Scientific distributed one FARASTAR Pulsed Field Ablation Generator with instructions that were missing information about the FARAPOINT PFA catheter. The incomplete labeling could affect proper device use and patient safety.
- 2026-07-29FDA-DeviceBoston Scientific CorporationClass IIBoston Scientific FARASTAR ablation generator recalled for incomplete instructions
Boston Scientific distributed 18 FARASTAR Ablation Generator units in Europe with incomplete Instructions For Use (IFU). The labeling did not include information about the FARAPOINT PFA catheter, which is used with the device. This discrepancy could affect proper device setup and use.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline surgical kits recalled for anesthetic quality issues
Medline Industries is recalling specific surgical convenience kits used in joint replacement procedures because they contain a pain-reliever medication (Bupivacaine Hydrochloride in Dextrose) with quality problems. The medication was manufactured by Huons Co, Ltd. and distributed through B. Braun Medical. The quality issues were identified by the supplier and no injuries have been reported.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline C-section kits recalled for anesthetic quality issues
Medline Industries is recalling specific C-section convenience kits (SKU DYNJ910835 and DYNJ910835A) that contain an anesthetic medication with quality problems. The anesthetic, Bupivacaine Hydrochloride in Dextrose Injection, was recalled by its manufacturer due to quality issues.
- 2026-07-29FDA-DeviceMedline Industries, LPClass IMedline Anterior Hip Kit recalled for anesthetic quality issues
Medline Industries is recalling specific Anterior Hip surgical kits (SKU DYNJ909640G) that contain a B. Braun convenience kit with Bupivacaine Hydrochloride in Dextrose Injection. The anesthetic component was manufactured by Huons Co, Ltd., which issued a voluntary recall due to quality concerns with the injectable drug.
- 2026-07-29FDA-DeviceWilcox Industries Corp.Class IIWilcox BOSS Xe aiming devices need safety software update
Wilcox Industries has released a software enhancement designed to increase the safety of its BOSS Xe aiming devices. The company is notifying all customers who purchased these products that the update should be installed.
- 2026-07-29USDAPublic Health AlertRed's All Natural steak burrito has undeclared egg
Red's All Natural Steak, Cilantro, and Lime Burritos contain egg, which is not listed on the package label. The product was mislabeled and a consumer discovered the mistake. The affected burritos were produced on June 19, 2026, and shipped to Costco locations in Illinois, Michigan, and Minnesota.
- 2026-07-29FDA-FoodMan Fon, Inc.Class IIMan Fon wonton wrappers recalled for undeclared wheat, dyes
Man Fon wonton wrappers were distributed without ingredient labels. The products contain wheat and artificial food colorings (Yellow #5 and Yellow #6) that are not declared on the packaging. People with wheat allergies or sensitivities to these dyes could have a serious reaction if they consume the product.
- 2026-07-29FDA-FoodMan Fon, Inc.Class IIMan Fon Won Ton Wrappers recalled for undeclared food dyes
Man Fon, Inc. recalled its Won Ton Wrappers Extra Thin (10 oz) because the product contains Yellow #5 and Yellow #6 food colorings that are not listed on the label. These dyes can cause allergic reactions in people sensitive to them. The affected product was distributed to restaurants in California and to grocery stores in New Mexico.
- 2026-07-29FDA-FoodGELLERT GLOBAL GROUPClass IFusia Kimchi & Tofu Kimbap recalled for undeclared fish
Fusia Kimchi & Tofu Kimbap and Spicy Tuna with Gochujang Kimbap frozen meals contain fish that is not declared on the label. People with fish allergies who eat this product could have a serious allergic reaction.
- 2026-07-29FDA-FoodTotal Nutrition IncClass ITNVitamins Moringa Capsules and Powder recalled for Salmonella
TNVitamins 100% Organic Moringa Capsules (1,200 mg) and Moringa Powder (96 grams) have been found to be contaminated with Salmonella. The contamination affects specific lot numbers: Capsules (Lot #2800, expires 2/2028) and Powder (Lot #2782, expires 5/2028). No illnesses have been reported to date.
- 2026-07-29FDA-FoodShandong Ling Xian Food Co.,LTDClass IIIIsland Pacific imitation crab flakes recalled for undeclared additive
Island Pacific imitation crab flakes (1.0 lb packages, UPC 0000000175012) contain sodium tripolyphosphate (STTP), a food additive that was not listed on the product label. The affected products have expiration dates of June 17 or 25, 2026; October 8, 2027; and March 5, 2028. About 751 cartons were distributed in California.
- 2026-07-29FDA-FoodShandong Ling Xian Food Co.,LTDClass IIINautilus imitation crab sticks recalled for undeclared additive
Nautilus imitation crab sticks (1.0 lb packages, UPC 878665000235) contain undeclared sodium tripolyphosphate (STTP), a food additive not listed on the label. The product was distributed in California. People with sensitivities to this ingredient may be affected.
- 2026-07-29FDA-FoodShandong Ling Xian Food Co.,LTDClass IIIIsland Pacific crab sticks recalled for undeclared additive
Island Pacific imitation crab sticks contain sodium tripolyphosphate (STTP), a food additive, that was not listed on the package label. The product was distributed in California. No injuries have been reported.