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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.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International peritoneal lavage kits recalled for sterility risk
Arrow International's 8FR peritoneal lavage catheter kits contain anesthetic medications (lidocaine and bupivacaine) from a supplier with known quality issues. If the sterility of these injectable components is compromised, patients could face serious injury or infection.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International JACC kits recalled for contaminated injectables
Arrow International JACC catheter kits contain lidocaine, bupivacaine, and sodium chloride from a supplier with quality control problems. The injectable components may not work properly or could be sterile-compromised, risking serious infection if used.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for contaminated components
Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with quality issues in multiple PICC and JACC catheter kits. The anesthetic and saline components may be ineffective or contaminated, which could cause serious infection or other life-threatening complications if used.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for contaminated components
Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with quality issues in multiple catheter and arterial line kits. The supplier's products showed signs of ineffectiveness and potential sterility problems, which could cause serious harm if compromised injectable products are used.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International CVC kits recalled for contaminated anesthetic drugs
Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with quality problems in multiple central venous catheter kits. The supplier's products had reports of ineffectiveness, and if sterility is compromised, these injectable drugs could cause serious infection or other life-threatening complications.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International CVC kits recalled for sterility concerns
Arrow International included anesthetic and saline components from a supplier with quality issues in several percutaneous central venous catheter (CVC) kits. The supplier's products showed limited reports of drug ineffectiveness, and compromised sterility in injectable products could cause serious injury.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for sterility concerns
Arrow International included injectable medications (lidocaine, bupivacaine, and sodium chloride) from a supplier with quality issues in several catheter kit models. If the sterility of these water-based injectable products is compromised, patients could face serious or life-threatening infections.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International hemodialysis kits recalled for contaminated solutions
Arrow International hemodialysis kits contain lidocaine, bupivacaine, and saline solution from a supplier with quality control problems. The contaminated materials may not work as intended, and compromised sterility in injectable products could cause serious harm to patients.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International hemodialysis kits recalled for sterility issues
Arrow International included injectable medications (lidocaine, bupivacaine, and sodium chloride) from a supplier with quality problems into hemodialysis kits. The supplier's products may not be sterile or effective, which could cause serious injury if used.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International epidural kits recalled for sterility concerns
Arrow International included anesthetic medications (lidocaine, bupivacaine) and saline from a supplier with quality issues in multiple epidural catheter kits. The supplier's products may not be sterile or effective, and compromised sterility in injectable products can cause serious infection or other life-threatening complications.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International PICC kits recalled for contaminated anesthetic components
Arrow International included lidocaine, bupivacaine, and saline solution from a supplier with quality issues in multiple PICC (peripherally inserted central catheter) kit models. The supplier's products may be ineffective or contaminated, and compromised sterility in injectable products can cause serious infection or injury.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for sterility risk
Arrow International recalled multiple central venous catheter kits that contain lidocaine, bupivacaine, and saline solution from a supplier with quality issues. The supplier's products may have compromised sterility, which could reduce drug effectiveness and pose serious health risks if the injectable solution is contaminated.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International catheter kits recalled for drug quality issues
Arrow International included lidocaine, bupivacaine, and saline solutions from a supplier with known quality problems in multiple arterial and radial artery catheter kits. The supplier's medications showed signs of ineffectiveness, and if the sterility of these injectable products was compromised, patients could face serious injury.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International PICC kits recalled for sterility concerns
Arrow International recalled several PICC (peripherally inserted central catheter) kits and stylets because they contain injectable medications from a supplier with quality issues. The medications—lidocaine, bupivacaine, and saline—may be ineffective or contaminated, which could cause serious injury if used.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International Pacing PSI Kits recalled for sterility and drug concerns
Arrow International included local anesthetic drugs (lidocaine and bupivacaine) from a supplier with quality issues into several pacing procedure kits. The supplier's drugs had limited reports of ineffectiveness, and compromised sterility in injectable products could cause serious infection or other life-threatening complications.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International biopsy kits recalled for anesthetic sterility issues
Arrow International included anesthetic medications (lidocaine and bupivacaine) and saline solution from a supplier with quality problems in its biopsy system kits. The supplier had reports of drug ineffectiveness, and compromised sterility in injectable products could cause serious injury.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International anesthesia kits recalled for contaminated solutions
Arrow International included lidocaine, bupivacaine, and saline solutions from a supplier with quality problems in multiple anesthesia and nerve block kits. The supplier's products may be ineffective or contaminated, which could cause serious infection or other life-threatening complications if the sterility of these injectable solutions is compromised.
- 2026-06-24FDA-DeviceARROW INTERNATIONAL, LLCClass IArrow International paracentesis kits recalled for sterility risk
Arrow International paracentesis kits (models AK-00376 and ASK-00376-VCU) contain anesthetic and saline solutions from a supplier with quality issues and reports of drug ineffectiveness. If the sterility of these injectable products is compromised, they could cause serious or life-threatening infections or complications during the procedure.
- 2026-06-24FDA-DeviceAbiomed, Inc.Class IAbiomed Impella Controller recalled for software error
A software error in certain Automated Impella Controller devices (used to manage left heart support blood pumps) may affect device function. The error affects controllers with software versions 6.0.1, 6.0.2, 6.0.3, 7.1 and above across multiple regions worldwide.
- 2026-06-24FDA-DeviceDatex-Ohmeda IncClass IDatex-Ohmeda Panda warmer recalled for oxygen concentration error
A blender component in certain Datex-Ohmeda Panda Freestanding Warmers can loosen over time, causing the device to deliver oxygen at a concentration that does not match the setting the user selected. This can result in infants receiving too much or too little oxygen, potentially causing harm.
- 2026-06-24FDA-DeviceDatex-Ohmeda IncClass IDatex-Ohmeda infant warmers recalled for oxygen delivery risk
A component in certain Giraffe and Panda warming systems can loosen during maintenance, causing the device to deliver oxygen at a concentration different from what the clinician set. This can result in too much oxygen (hyperoxia) or too little oxygen (hypoxia) being delivered to the patient.
- 2026-06-24FDA-DeviceDatex-Ohmeda IncClass IDatex-Ohmeda Giraffe resuscitator recalled for oxygen delivery risk
A component in certain Giraffe Stand-alone Infant Resuscitation Systems can loosen during maintenance, causing the device to deliver oxygen at the wrong concentration. Infants may receive too much or too little oxygen, risking serious harm.
- 2026-06-24FDA-FoodDkiru LLCClass IIAdndale Magnesium Glycinate Gummies recalled for undeclared melatonin
Dkiru LLC's Adndale Magnesium Glycinate Gummies 400 mg contain melatonin that is not listed on the label. The affected product is sold in 90-count plastic bottles (UPC 860008784551) with three affected lot numbers expiring between August and September 2026. Melatonin is a sleep aid not declared in the ingredient list, which poses a risk to consumers who may not expect it or who should avoid it due to other medications or health conditions.
- 2026-06-24FDA-FoodInternational Food Products CorporationClass IIDairy House Strawberry Dairy Powder recalled for Salmonella risk
Dairy House Ingredient Systems Strawberry Dairy Powder in 50 lb bags may be contaminated with Salmonella. The affected product (Lot #26126A6A, use by date 2027-05-06) was distributed to Texas, Tennessee, and Oklahoma.
- 2026-06-24FDA-FoodInternational Food Products CorporationClass IIDairy House Vanilla Dairy Powder recalled for Salmonella risk
Dairy House Ingredient Systems Vanilla Dairy Powder in 50 lb boxes may be contaminated with Salmonella. The affected product was distributed to food service and manufacturing customers in Texas, Tennessee, and Oklahoma.
- 2026-06-24FDA-FoodInternational Food Products CorporationClass IILegacy Tex Dressing Stabilizer Blend recalled for Salmonella
International Food Products Corporation's Legacy Tex Dressing Stabilizer Blend #7604-50 tested positive for Salmonella. The contaminated product was distributed in Texas, Tennessee, and Oklahoma. Affected lot 26121A6A (item #502574) has a use-by date of May 4, 2027.
- 2026-06-24FDA-FoodAzuma Foods International Inc USAClass IAzuma Foods Tako Wasabi recalled for undeclared fish
Azuma Foods Tako Wasabi seasoned octopus contains fish that is not declared on the label. People with fish allergies could have a serious allergic reaction if they eat this product. The recall affects frozen retail packs and foodservice units distributed across multiple states.
- 2026-06-24FDA-FoodJonco IndustriesClass IFireworks Popcorn White Cheddar Seasoning recalled for Salmonella risk
Fireworks Popcorn White Cheddar Seasoning was made with recalled California Dairies milk powder that may contain Salmonella. The affected seasoning was sold in multiple sizes, including gift sets from Fireworks Popcorn and Williams Sonoma, primarily distributed in Wisconsin and Mississippi.
- 2026-06-24FDA-FoodUnited Salt CorpClass IIIUnited Salt Corp salt recalled for incorrect labeling
United Salt Corp salt products were labeled incorrectly: some plain salt was labeled as iodized, and some iodized salt was labeled as plain. This labeling error means customers may not know whether their salt contains iodine, which is important for those managing their iodine intake for health reasons.
- 2026-06-24FDA-FoodFairhope Roasting CompanyClass IIFairhope Roasting Company cold brew concentrate recalled for missing refrigeration label
Fairhope Roasting Company Cold Brew Coffee Concentrate in 1-gallon jugs is missing a "Keep Refrigerated" statement on the label, even though the product requires refrigeration to stay safe. This labeling error could lead to improper storage and potential spoilage or foodborne illness. The affected batches were distributed to food service operations in Alabama.