Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 451–500 of 17,395

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  SOUP MIX-6/58oz Tray, PPS971 CLR PET 900/cs 32cs/pal, film-sealed (18" 16 Micron Perserva Wrap 5000/rl), packed in 30# Kale 44ect

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  HEB-GUAC KIT-MILD-3/57.5oz

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  PICO DE GALLO-MILD-4oz PICO DE GALLO-MILD-6/14oz PICO DE GALLO-4/5# PICO DE GALLO-1/5# PICO DE GALLO-MILD-1/5#

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Food Recall · August 5, 2026

  NatureBest Pre-Cut & Produce LLc

  HEB-PICO-MEDIUM-12/14oz PICO DE GALLO-MEDIUM-6/14oz PICO DE GALLO-MEDIUM-6/9oz PICO-DE-GALLO-MEDIUM-BGC-1/5# PICO-MEDIUM-SNACK-12/4oz

  Jalapenos have the potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · August 5, 2026

  Nipro Renal Soultions USA, Corporation

  MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201

  Hemodialysis concentrates contain high endotoxin levels

  Class II

• Food Recall · August 5, 2026

  GET FRESH PRODUCE

  Get Fresh Produce Jalapeno Peppers. Item 01896 - 2 lb. box; Item 01894 - 10 lb. box

  Potential Salmonella contamination

  Class I

• Food Recall · August 5, 2026

  Sirna and Sons Produce, Inc

  Sirna & Sons Produce PEPPER JALAPENO BREAK 1LB, repackaged into 1 lb. plastic bags, Product Number: 55255, Packed by Sirna & Sons Produce 7176 State Route 88, Ravenna, OH 44266, distributed for food s

  Potential Salmonella Javiana contamination

  Class I

• Medical Device Recall · August 4, 2026

  B Braun Medical Inc

  Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025

  Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.

  Class II

• Drug Recall · August 4, 2026

  Novartis Pharmaceuticals Corporation

  Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 007

  Failed Dissolution Specifications

  Class II

• Drug Recall · August 4, 2026

  Fresenius Kabi USA, LLC

  Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only, Fresenius Kabi, Lake Zurich, IL. Unit of Use NDC Number 76045-00

  Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.

  Class I

• Medical Device Recall · August 4, 2026

  Canon Medical System, USA, INC.

  Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicat

  Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.

  Class II

• Medical Device Recall · August 4, 2026

  PTW FREIBURG

  Brand Name: VERIQA; Product Name: RT MonteCarlo 3D v3; Model/Catalog Number: S070031.520; Software Version: 3.1.18;

  When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorrectly omit the bolus during treatment and deliver the prescribed dose to the wrong tissue depth.

  Class II

• Food Recall · August 4, 2026

  H & U Inc. dba Sun Noodle

  Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen noodle kit which contains noodles and Soba soup packet. Item #05410 retail packa

  Soba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on finished product label.

  Class I

• Medical Device Recall · August 3, 2026

  Baxter Healthcare Corporation

  Brand Name: VOLARA System Product Name: VOLARA, HC, NA A Model/Catalog Number: M08594A Software Version: N/A Product Description: VOLARA, HOMECARE, NORTH AMERICA Component: No

  Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and testing confirmed devices meet specifications.

  Class II

• Drug Recall · August 3, 2026

  Lupin Pharmaceuticals Inc.

  Clobetasol Propionate Cream USP, 0.05%, 60 g tube, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, United States, Manufactured by: Lupin Limited, Pithampur (MP) 454 775, INDI

  Failed content uniformity specifications.

  Class II

• Drug Recall · August 3, 2026

  Shoolin Pharma Chem LLP

  SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-bag Net Wt, RX ONLY "FOR Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mah

  CGMP Deviations:Noted during FDA inspection

  Class II

• Food Recall · August 3, 2026

  Nutrient Foods, LLC

  Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalized poly pillow pouch. Net wt.8.9 oz (252g). 1 pillow pouch per kit. Nutrient, 110 Woodland Ave Reno,

  Soy not declared in the contains statement.

  Class II

• Drug Recall · August 3, 2026

  Shoolin Pharma Chem LLP

  TADALAFIL USP, 0.100 KG, 0.1KG(100gm)-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,

  CGMP Deviations:Noted during FDA inspection

  Class II

• Drug Recall · August 3, 2026

  SUN PHARMACEUTICAL INDUSTRIES INC

  Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Distributed by: Taro Pharmaceuticals USA, Inc., Hawthor

  CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing

  Class II

• Drug Recall · August 3, 2026

  Shoolin Pharma Chem LLP

  TADALAFIL USP, 0.500 KG, 0.500KG(500gm)-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

  CGMP Deviations:Noted during FDA inspection

  Class II

• Drug Recall · August 3, 2026

  Shoolin Pharma Chem LLP

  SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mah

  CGMP Deviations:Noted during FDA inspection

  Class II

• Drug Recall · August 3, 2026

  Shoolin Pharma Chem LLP

  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, Gu

  CGMP Deviations:Noted during FDA inspection

  Class II

• Food Recall · August 1, 2026

  EURO FOODS GROUP USA NJ INC

  Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen

  The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

  Class I

• Food Recall · August 1, 2026

  Blank Slate Creamery Production

  Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic package

  undeclared egg

  Class I

• Medical Device Recall · July 31, 2026

  GE Healthcare

  Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions

  Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

  Class II

• Medical Device Recall · July 31, 2026

  Bayer Medical Care, Inc.

  MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;

  Some devices may not have been properly sterilized due to a manufacturing sterilization issue.

  Class II

• Medical Device Recall · July 31, 2026

  Johnson & Johnson Surgical Vision, Inc.

  HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF: 10301012 (EU); HEALON DUET PRO II, REF: 10301016 (EU)

  Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during insertion, withdraw cannula and reassess the insertion conditions (i.e. insertion angle, incision size, etc.) before proceeding because forcing the cannula may cause corneal abrasion, iris trauma or descemet's membrane detachment.

  Class II

• Medical Device Recall · July 31, 2026

  Maquet Cardiopulmonary Gmbh

  Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS);

  The packaging may not consistently maintain sterile barrier integrity.

  Class II

• Medical Device Recall · July 31, 2026

  GE Healthcare

  Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions

  Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

  Class II

• Medical Device Recall · July 31, 2026

  Medline Industries, LP

  Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A

  Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

  Class II

• Medical Device Recall · July 31, 2026

  GE Healthcare

  Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions

  Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

  Class II

• Medical Device Recall · July 31, 2026

  WELL LEAD MEDICAL CO. LTD

  SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25

  The 6Fr suction catheter could not pass through the samples smoothly.

  Class II

• Medical Device Recall · July 31, 2026

  Philips North America

  Philips Patient Information Center iX REF:866389

  Due to software malfunction, patient information system may freeze and become unresponsive.

  Class II

• Medical Device Recall · July 31, 2026

  Maquet Cardiopulmonary Gmbh

  Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);

  The packaging may not consistently maintain sterile barrier integrity.

  Class II

• Medical Device Recall · July 31, 2026

  Medline Industries, LP

  Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F

  Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

  Class II

• Medical Device Recall · July 31, 2026

  GE Healthcare

  Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applic

  Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

  Class II

• Medical Device Recall · July 31, 2026

  New York Embroidery Studio, Inc.

  New York Embroidery Studio Trinity Non-Surgical Isolation Gown, AAMI PB70 Level 2, X-Large. Model Number: NYES100-2. Packaged in inner packs of 10 and 100 gowns per shipping case.

  Gowns do not consistently meet the minimum liquid-barrier performance required.

  Class II

• Medical Device Recall · July 31, 2026

  Medline Industries, LP

  Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A

  Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

  Class II

• Medical Device Recall · July 31, 2026

  Medline Industries, LP

  Convenience kits CATARACT PACK DYNJ59881A

  Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

  Class II

• Medical Device Recall · July 31, 2026

  Maquet Cardiopulmonary Gmbh

  Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);

  The packaging may not consistently maintain sterile barrier integrity.

  Class II

• Medical Device Recall · July 31, 2026

  GE Healthcare

  Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation, distribution, printing, editing, and processing of digital images an

  Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

  Class II

• Drug Recall · July 31, 2026

  Liebel-Flarsheim Company LLC

  Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufactured by: Liebel-Flarsheim Company LLC, Ralei

  Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.

  Class I

• Medical Device Recall · July 31, 2026

  GE Healthcare

  Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions

  Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.

  Class II

• Medical Device Recall · July 31, 2026

  Philips North America

  Philips PIC iX Essentials REF:867093

  Due to software malfunction, patient information system may freeze and become unresponsive.

  Class II

• Medical Device Recall · July 30, 2026

  Howmedica Osteonics Corp.

  SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components manufactured from UHMWPE (polyethylene)

  Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

  Class II

• Medical Device Recall · July 30, 2026

  Datex-Ohmeda, Inc.

  Aisys, Datex-Ohmeda anesthesia system, Part Number 1011-9050-000

  Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician intervention. If this is not provided, the patient may experience decreased anesthetic agent effect.

  Class II

• Medical Device Recall · July 30, 2026

  Howmedica Osteonics Corp.

  ACETABULAR CUP UHMWPE 61-3258 ALL POLY CONSTRAINED INSERT 44MM 69-2244 ALL POLY CONSTRAINED INSERT 46MM 69-2246 ALL POLY CONSTRAINED INSERT 48MM 69-2248 ALL POLY CONSTRAINE

  Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

  Class II

• Vehicle Recall · July 30, 2026

  Honda (American Honda Motor Co.)

  2023 HONDA CMX300, 2023 HONDA CMX500

  A detached screw may lodge between the frame and stem, interfering with steering and increasing the risk of a crash or injury.

  Unclassified

• Medical Device Recall · July 30, 2026

  Howmedica Osteonics Corp.

  DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-800 C-M062-7-500 C-M063-2-600 SELF-PRESSURIZING GLENOID SIZE 9 C-M063-5-000 SHOULDER

  Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

  Class II

• Medical Device Recall · July 30, 2026

  Howmedica Osteonics Corp.

  ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNEE P/S 82-3-0318 SCORPIO + MOBILE BEARING PCS 78-5-0910 SCORPIO C-DOME PATELLA

  Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

  Class II