Safety Recalls

15,184 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,951–2,000 of 15,184

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Jalapeno Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Whipped Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Caramel Apple Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Jalapeno Cheddar Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Consumer Product Recall · February 19, 2026

  Prismatic 3D Prints LLC of Loveland, Colorado

  Prismatic 3D Prints Book Nooks with Lights

  The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium coin battery that can be easily accessed by children. In addition, the spare coin battery is not in child resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · February 19, 2026

  Shenzhenshilonghuaqujialebeibaihuoshanghang (Jialebei Department Store, Longhua District, Shenzhen) dba Samit Outdoor, of China

  SAMIT Youth Multi-Purpose Helmets

  The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

  Unclassified

• Food Recall · February 19, 2026

  Willamette Valley Pie Company, LLC

  Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold

  Potential contamination with listeria monocytogenes.

  Class II

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Tofu Whipped; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Strawberry Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Consumer Product Recall · February 19, 2026

  Shenzhen Huakechuang Technology Co. Ltd., dba Huaker, of China

  Huaker Magnetic Balls and Rods Sets

  The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

  Unclassified

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Blueberry Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Scallion Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Garlic & Herb Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Lox Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Vegetable Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Drug Recall · February 19, 2026

  Radnostix

  Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 692

  Failed Tablet/Capsule Specifications

  Class III

• Food Recall · February 19, 2026

  Made Fresh Salads Inc

  Made Fresh Salads brand Apple Cinnamon Cream Cheese; 5 lb white plastic tub

  Products may be contaminated with Listeria monocytogenes.

  Class I

• Food Recall · February 19, 2026

  Willamette Valley Pie Company, LLC

  Frozen Raw Bulk 8 inch Blueberry Crumble Pie (4 pies/case). Net wt. 24.5oz. UPC 0002251881223. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen Raw pies were sold fr

  Potential contamination with listeria monocytogenes.

  Class II

• Food Recall · February 19, 2026

  Super World Trading Inc.

  MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months;

  Products contain cyclamates (banned sweetener)

  Class III

• Food Recall · February 19, 2026

  Super World Trading Inc.

  MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd;

  Products contain cyclamates (banned sweetener)

  Class III

• Food Recall · February 19, 2026

  Super World Trading Inc.

  MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Liquorice, Sugar, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufa

  Products contain cyclamates (banned sweetener)

  Class III

• Consumer Product Recall · February 19, 2026

  Shenzhen Yimu Technology Co., Ltd. dba JJGoo, of China

  JJGoo LED Balloon Lights

  The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · February 19, 2026

  Joly's LLC, of Orlando, Florida

  Joly's 80% Vinegar (32 oz, pack of two)

  The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance lacks required warning labels and first-aid treatment instructions. This poses a deadly risk of poisoning if the contents are swallowed and a serious injury from chemical burns to the skin and eyes if improperly handled.

  Unclassified

• Medical Device Recall · February 18, 2026

  Stryker Medical Division of Stryker Corporation

  Cub Pediatric Crib, Model FL19H

  Cribs sold in the USA are missing two access door warning labels.

  Class II

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc,

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Drug Recall · February 18, 2026

  HTO Nevada Inc. dba Kirkman

  MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.

  Stability Data Does Not Support Expiry Date.

  Class II

• Drug Recall · February 18, 2026

  Cipla USA, Inc.

  Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, Outer carton: 112 capsules (4 individua

  Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.

  Class III

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-157LH Smooth Low Height Tissue Expander, 650cc

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH, SCPX-123TH, SCPX-140TH, SCPX-146TH Smooth Tall Height Tissue Expander, 350cc, 450cc, 650cc, 750cc

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Drug Recall · February 18, 2026

  Cipla USA, Inc.

  Nilotinib Capsules, 150 mg per capsule, packaged in cartons, Rx only, Manufactured by: Cipla Ltd., Verna, Goa, India, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, N

  Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.

  Class III

• Medical Device Recall · February 18, 2026

  Baxter Healthcare Corporation

  Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.

  Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use.

  Class I

• Drug Recall · February 18, 2026

  HTO Nevada Inc. dba Kirkman

  MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.

  Stability Data Does Not Support Expiry Date.

  Class II

• Drug Recall · February 18, 2026

  HTO Nevada Inc. dba Kirkman

  FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.

  Stability Data Does Not Support Expiry Date.

  Class II

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Medical Device Recall · February 18, 2026

  Medline Industries, LP

  Sterile Radiology Procedure Kits, Model Number DYNDH1491B

  There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.

  Class II

• Medical Device Recall · February 18, 2026

  Abiomed, Inc.

  Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding product codes. 1. Purge Cassette, 5 Pack; Product Code

  Increased risk of purge leaks with Generation 1 purge cassettes.

  Class I

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Medical Device Recall · February 18, 2026

  Hologic, Inc.

  Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No

  Due to product exhibiting potential to generate either invalid or false negative results.

  Class II

• Medical Device Recall · February 18, 2026

  Navajo Manufacturing Company

  Handy Solutions Neck & Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd

  If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property.

  Class I

• Medical Device Recall · February 18, 2026

  Mentor Texas, LP.

  Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600

  Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

  Class II

• Medical Device Recall · February 18, 2026

  XTANT Medical Holdings, Inc

  XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.

  Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.

  Class II

• Food Recall · February 18, 2026

  NRS Enterprises, Inc. dba Sunflour Bakery

  Sunflour Bakery Hamburger Bun, 18oz plastic bag containing 6 buns. UPC- 832971001522

  Undeclared sesame seed ingredient in hamburger buns.

  Class II

• Medical Device Recall · February 18, 2026

  Elekta, Inc.

  Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekt

  Due to adapter not being properly aligned or locked in place.

  Class II

• Medical Device Recall · February 18, 2026

  Baxter Healthcare Corporation

  Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Visi

  Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.

  Class II

• Food Recall · February 17, 2026

  Wawa Beverage Company

  Wawa Cookies & Cream Milk 16 oz (Pint), Plastic bottle Store Refrigerated

  Foreign plastic material discovered on fill line.

  Class II

• Food Recall · February 17, 2026

  Wawa Beverage Company

  Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated

  Foreign plastic material discovered on fill line.

  Class II

• Drug Recall · February 17, 2026

  The Harvard Drug Group LLC

  Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6818-06.

  Defective container; inadequately sealed blister packaging.

  Class II

• Medical Device Recall · February 17, 2026

  Molded Products Inc

  See Luer Cap Set, MPC-130, set, administration, intravascular

  Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.

  Class II

• Food Recall · February 17, 2026

  Wawa Beverage Company

  Wawa Reduced Fat Milk 2% 16 oz (Pint)

  Foreign plastic material discovered on fill line.

  Class II