Safety Recalls

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

Showing 651–700 of 17,395

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT DYKS1476A

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT PREOP KIT DYKS1583A

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN HEART CDS983348AA CDS983348AB

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  GE Medical Systems Information Technologies Inc

  PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353

  Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators C-SECTION PREP DYNJ32702B

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  GE Medical Systems Information Technologies Inc

  PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209

  Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

  Class II

• Medical Device Recall · July 20, 2026

  Mirion Technologies (Capintec), Inc.

  Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;

  Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DYNJ42828B EYE BASIN TRAY-LF DYNJ42832B

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START KIT LAB DRAW-SH CDS860014Q IV START KIT DYKM1000B IV START KIT LAB DRAW-SH CDS860014P ULTRASOUND

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  Medline Industries, LP

  Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators DELUXE PRE OP KIT DYKS2018 GENERAL PREOP KIT DYKS1584A PRE OP KIT DYKS1216I PRE-OP KIT DYKM1398B

  Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

  Class II

• Medical Device Recall · July 20, 2026

  GE Medical Systems Information Technologies Inc

  PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592

  Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

  Class II

• Medical Device Recall · July 20, 2026

  GE Medical Systems Information Technologies Inc

  FRU (Field replaceable unit), PORTRAIT CORE SERVICES SW RELOAD V1.1, Ref# 5700225

  Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.

  Class II

• Medical Device Recall · July 20, 2026

  Midmark Corporation

  Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.

  A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.

  Class II

• Food Recall · July 20, 2026

  Piazza Produce (dba CIBUS Fresh)

  Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253

  Possible Cyclospora Contamination

  Class I

• Food Recall · July 19, 2026

  FACTORY6, INC.

  Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for

  Possible Salmonella in Moringa Leaf Powder product.

  Class I

• Food Recall · July 18, 2026

  M.G. Foods, Inc.

  Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2 oz (232g) UPC 1 00001 00029 7 and Sprig & Sprout Spicy Breakfast Burrito IN A SPIC

  Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  SYSCO LETTUCE SALAD MIX 4/5# SYSCO LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  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.

  Potential Cyclospora contamination.

  Class I

• Medical Device Recall · July 17, 2026

  Remel Europe Ltd.

  Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics

  Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.

  Class II

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  MARKON BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  TAYLOR FARMS LETTUCE SALAD W/BAG 4/5# Iceberg, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  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 68

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  SUBWAY SHRED LETTUCE 1/4" 4/5# Iceberg only products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  Jack in the Box 1/8" SHRED LETTUCE 4/5# Iceberg only products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  MARKON LETTUCE SALAD MIX 4/5# MARKON LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  Cross Valley Farms BLEND LETT/ROM 80/20 WITH SEP BAGGIES 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Drug Recall · July 17, 2026

  Sunny Pharmtech Inc.

  Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1

  Presence of Particulate Matter; identified as stainless steel

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  PEAK LETTUCE SHRED 1/8" 4/5# Iceberg only products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  TAYLOR FARMS BLEND LETT/ROM BLEND WITH BAG 4/5# Iceberg, Romaine, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  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"

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  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# TA

  Potential Cyclospora contamination.

  Class I

• Drug Recall · July 17, 2026

  Sunny Pharmtech Inc.

  Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1

  Presence of Particulate Matter; identified as stainless steel

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  Cross Valley Farms LETTUCE SALAD MIX 4/5# Cross Valley Farms LETTUCE SALAD WITH SEP BAG 4/5# Iceberg, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  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.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  YUM LETTUCE SHREDDED 1/4" 6/5# Iceberg only products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  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.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  PEAK LETTUCE SALAD W/BAG 4/5# Iceberg, Carrots, Red Cabbage products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Taylor Farms de Mexico S. de R.L. de C.V.

  SYSCO LETTUCE CHOP 4/5# SYSCO LETTUCE SHRED 1/8" 4/5# Iceberg only products.

  Potential Cyclospora contamination.

  Class I

• Food Recall · July 17, 2026

  Botticelli Foods, LLC

  bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g), UPC 194346207961

  Product may be contaminated with Salmonella.

  Class I

• Medical Device Recall · July 16, 2026

  Biofire Defense

  FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test intended

  Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based in vitro diagnostic panel test.

  Class II

• Medical Device Recall · July 16, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  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 ar

  Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2) Potential loss of geometry movements that may lead to delay of therapy and procedural complications

  Class II

• Medical Device Recall · July 16, 2026

  Straumann USA LLC

  Straumann Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim (Article 021.5314); implant, endosseous, root-form

  Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest.

  Class II

• Vehicle Recall · July 16, 2026

  International Motors, LLC

  2023 INTERNATIONAL MV, 2025 INTERNATIONAL MV, 2026 INTERNATIONAL MV

  A short circuit increases the risk of a fire.

  Unclassified

• Vehicle Recall · July 16, 2026

  Jaguar Land Rover North America, LLC

  2023 LAND ROVER DISCOVERY, 2024 LAND ROVER DISCOVERY

  A rearview camera image that does not display can decrease the driver's visibility, increasing the risk of a crash.

  Unclassified

• Consumer Product Recall · July 16, 2026

  Panasonic Manufacturing (Xiamen) Co., Ltd, of Xiamen, Fujian, China

  Electric Toaster Ovens

  The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.

  Unclassified

• Vehicle Recall · July 16, 2026

  International Motors, LLC

  2025 IC BUS CESB

  The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.

  Unclassified

• Drug Recall · July 16, 2026

  Ascend Laboratories, LLC

  Dabigatran Etexilate Capsules, 75 mg, 60-count (6x10)blister pack further packaged in a carton, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, INDIA, Distributed by: MAJOR PHARMACEUTICALS,

  Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability

  Class III

• Drug Recall · July 16, 2026

  Fresenius Kabi USA, LLC

  Naropin (ropivacaine hydrochloride Injection, USP), 0.5%, 100 mg per 20 mL (5 mg per mL), Twenty-five, 20 mL Single-Dose Vials, Rx only, Fresenius Kabi, Lake Zurich, IL 60047 NDC Tray: 63323-286-23; N

  Presence of Particulate Matter: Hair was found in products

  Class II