Recalls in April 2026 (page 3)
673 recalls.
- TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - TDC VELOCE" recall (D.O.R.C. Dutch Opthalmic Research Center Intl B.V.)
Medical deviceClass IIReported June 17, 2026 · An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. - EXCOR Pediatric Ventricular Assist Device recall (BERLIN HEART GMBH)
Medical deviceClass IIReported June 17, 2026 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures. - Mahurkar Elite PASS Trays recall (Mozarc Medical US LLC)
Medical deviceClass IIReported June 17, 2026 · The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays. - Allia Moveo angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 7 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 5 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 3 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Plum Duo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100 recall (Fresh Roast Systems Inc)
Medical deviceClass IIReported June 17, 2026 · A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific... - Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g recall (Nassar Investment Company LLC)
FoodClass IReported June 10, 2026 · Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella. - cafe nouria blueberry muffin recall (The Brownie Baker Inc.)
FoodClass IIReported June 10, 2026 · Undeclared walnuts - Brand Name: Da Vinci 5 Product Name: ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported June 10, 2026 · Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions... - Sharpoint 2.2MM recall (SSC- Surgical Specialties Corporation)
Medical deviceClass IIReported June 10, 2026 · 3.0mm surgical knives labeled and packaged as 2.2mm surgical knives. - TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 ... recall (Grace Medical, Inc.)
Medical deviceClass IIReported June 10, 2026 · Due to incorrect functional length on device labeling. - Aligned Medical AMS16835 Fluids Kit RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported June 10, 2026 · Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits. - MAC 5 A4 Resting ECG Analysis System 855001-001 recall (GE Medical Systems China Co., Ltd.)
Medical deviceClass IIReported June 10, 2026 · Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with... - BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis Mini Main REF: 349 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedStation ES REF: 323 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - BD Pyxis MedStation 4000 REF: 303 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIReported June 10, 2026 · Fingerprint scanner may overheat to a temperature to cause 1st degree burn. - Avanta Multi-Patient Administration Tube Sets recall (Bayer Medical Care, Inc.)
Medical deviceClass IIReported June 10, 2026 · Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports... - Digital Angiography System Trinias:UD150G-40 / D150GC-40 recall (Shimadzu Medical Systems)
Medical deviceClass IIReported June 10, 2026 · Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off. - Arvis Hip & Knee 2.0 Instrument Set recall (Kico Knee Innovation Company)
Medical deviceClass IIReported June 10, 2026 · The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face. - Arvis Hip & Knee 3.0 Instrument Set recall (Kico Knee Innovation Company)
Medical deviceClass IIReported June 10, 2026 · The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face. - Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus... recall (Advanced Bionics, LLC)
Medical deviceClass IIReported June 10, 2026 · Due to incorrect shelf-life expiration date. - Covidien EndoStitch" Polysorb Single Use Loading Unit recall (Covidien, LP)
Medical deviceClass IIReported June 10, 2026 · The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure. - CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 10, 2026 · Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer... - PhaseOne Antimicrobial Solution recall (Oculus Technologies of Mexico, S.A. de C.V.)
Medical deviceClass IIReported June 10, 2026 · The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material... - Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050 recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance. - Covidien Mon-a-Therm General Purpose Temperature Probe REF: 90044 recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance. - Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: 90042 recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Temperature probe devices lack FDA clearance. - Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number:... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported June 10, 2026 · Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow... - COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code:... recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Due to customer complaint regarding incorrect display box labeling. - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in. recall (Becton Dickinson & Company)
Medical deviceClass IReported June 10, 2026 · This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to... - Wawa Fruit Punch Pint recall (Wawa Beverage Company)
FoodClass IReported June 3, 2026 · Undeclared Milk Allergen, - Wawa Diet Lemonade Pint recall (Wawa Beverage Company)
FoodClass IReported June 3, 2026 · Undeclared Milk Allergen, - Wawa Diet Iced Tea Lemon Pint recall (Wawa Beverage Company)
FoodClass IReported June 3, 2026 · Undeclared Milk Allergen, - Wawa Iced Tea Lemon 16 oz Pint recall (Wawa Beverage Company)
FoodClass IReported June 3, 2026 · Undeclared Milk Allergen, - (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099 recall (Honeyville, Inc)
FoodClass IReported June 3, 2026 · Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products. - Medline medical convenience kit labeled as EYE TRAY-LF recall (Medline Industries, LP)
Medical deviceClass IIReported June 3, 2026 · Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because... - Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - GE HealthCare ApexPro v6.0 eDelivery Software recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 3, 2026 · GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0... - GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 3, 2026 · GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0... - GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 3, 2026 · GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0... - GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 3, 2026 · GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0... - GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable... recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 3, 2026 · GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0... - GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported June 3, 2026 · GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0... - HydroMARK Breast Biopsy Site Marker recall (Devicor Medical Products Inc)
Medical deviceClass IIReported June 3, 2026 · Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers. - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 recall (O&M HALYARD INC)
Medical deviceClass IIReported June 3, 2026 · Nitrile Exam Glove failed to meet specifications chemical permeation performance. - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 3, 2026 · A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates... - RelayPro Thoracic Stent-Graft System recall (Bolton Medical Inc.)
Medical deviceClass IReported June 3, 2026 · Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PREMIUM HOT COCOA MIX recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA recall (Ghirardelli Chocolate Company)
FoodClass IReported May 27, 2026 · Potential contamination with Salmonella. - Pork King Good Onion & Sour Cream Seasoning. Net Wt. 3 oz recall (Pork King Good, LLC)
FoodClass IReported May 27, 2026 · Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination. - Solina 6022487 Garlic Herb Topping recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - YT 6027393 Spicy Ranch Blend recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6036087 Cr¿me Fraiche Spice Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6036277 Garlic Cream Sauce Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6036786 Instant Country Gravy Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6036554 Parmesan Breadstick Sauce Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6036443 Cheddar Cheese Powder Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6036195 Ranch Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6035687 Bayou Blackened Ranch Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Solina 6035415 Sourdough Cheese Crouton Seasoning recall (Solina U.S. Holding)
FoodClass IReported May 27, 2026 · potential to be contaminated with Salmonella - Non Fat Dry Milk 1# recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - PSW21585 Save A Lot Bind 50# recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination.