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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.

• 2026-10-27FDA-PRTaylor Farms
  H-E-B Chop Salad kit recalled for undeclared soy and almonds

  Taylor Farms is recalling H-E-B Backyard BBQ Chop Salad Kit (13.4 oz) because it may contain soy and tree nuts (almonds) that are not listed on the label. People with a soy or almond allergy could have a serious reaction if they eat it. No reactions have been reported so far.

• 2026-10-27FDA-PRHAIFA SMOKED FISH
  Haifa Smoked Fish cold smoked sprats recalled for botulism risk

  Haifa Smoked Fish of Queens, NY is recalling about 560 pounds of cold smoked sprats because they may be contaminated with Clostridium botulinum, the bacterium that causes botulism. The sprats were sold at retail stores in New Jersey, New York, and Pennsylvania. The company has reported no illnesses to date.

• 2026-10-26FDA-DevicePhilips North AmericaClass II
  Philips Model 712010 device recalled for failure risk

  Philips North America has recalled Model 712010 devices due to a potential for the device to fail immediately after exposure, which could cause the system to stop working. Approximately 563 units are affected.

• 2026-10-26FDA-DrugPar Health USA, LLCClass I2 products
  Par Health USA Argatroban Injection recalled for particulate matter

  Par Health USA's Argatroban Injection vials contain unwanted particles—including cellulose, polystyrene, plastic, stainless steel, or rubber stopper material—in the solution. The contamination affects multiple lot numbers distributed nationwide. No injuries have been reported.

• 2026-10-26FDA-DrugProdose, Inc.Class III
  ValuHealth acetaminophen recalled for mismatched bottle label

  ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg bottles have an incorrect label on the bottle itself. The outer carton correctly says "Acetaminophen 500 mg," but the label on the bottle says "Pain Relief PM" — a different product. This mismatch could cause confusion about what you're taking.

• 2026-10-26FDA-DrugHuons Co., Ltd.Class II
  Huons lubricant eye drops recalled for plastic contamination

  Huons carboxymethylcellulose sodium lubricant eye drops in single-use containers were found to contain a plastic-related compound (polyethylene leachable) at levels above acceptable limits. The contamination was detected during quality testing. Affected lots have expiration dates ranging from March 2027 to October 2028.

• 2026-10-26FDA-DrugSTRIDES PHARMA INCClass II
  Strides Pharma Cinacalcet tablets recalled for dissolution failure

  Strides Pharma is recalling one lot of Cinacalcet 30 mg tablets because they failed to meet dissolution specifications, meaning the tablets may not break down properly in the body. This could result in inconsistent or reduced drug effectiveness. The affected lot is 7717825A, expiring 11/30/2028.

• 2026-10-26FDA-DrugMACLEODS PHARMA USA, INCClass II
  Macleods Pharma blood pressure tablets recalled for dissolution failure

  Macleods Pharma USA is recalling specific lots of Olmesartan Medoxomil, Amlodipine, and Hydrochlorothiazide combination tablets (40 mg/10 mg/12.5 mg) because they failed to meet dissolution specifications. This means the tablets may not break down properly in the body, potentially reducing how well the medication works.

• 2026-10-24FDA-PRTonight We Ride, LLC
  Ultimate Forza male supplement recalled for hidden prescription drugs

  Tonight We Ride, LLC recalled all lots of Ultimate Forza Male Supplement capsules because they contain three undeclared active ingredients: sildenafil and tadalafil (prescription drugs sold as Viagra and Cialis) and dapoxetine (not approved by the FDA). These ingredients were found through third-party testing and pose health risks, especially for people taking nitrate medications or with heart conditions.

• 2026-10-24USDAClass I
  Imperio beef jerky recalled for lack of inspection

  Imperio Distribution LLC recalled approximately 946 pounds of ready-to-eat beef jerky products packaged between January and October 2026 because they were produced without federal inspection. The products also carried an unauthorized USDA inspection mark. These items were distributed to retailers in Illinois, Indiana, Iowa, Michigan, Minnesota, Missouri, and Wisconsin.

• 2026-10-23FDA-DeviceZIEHM-ORTHOSCAN INCClass II
  Ziehm Orthoscan VERSA cart recalled for monitor arm separation

  Certain Ziehm Orthoscan VERSA accessory carts and Versa Mini C-Arm systems have welds that do not meet specifications. This defect could cause the monitor arm mounting structure to separate from the cart during use.

• 2026-10-23FDA-DeviceMedtronic, Inc.Class II
  Medtronic OmniaSecure lead recalled for implant fixation difficulty

  Medtronic has recalled certain OmniaSecure Model 3930M ventricular leads (used in heart devices for pacing and defibrillation) due to reports of difficulty achieving proper fixation during implantation. This implantation difficulty could potentially cause tissue trauma during the surgical procedure.

• 2026-10-23FDA-DeviceEthicon, LLCClass II
  Ethicon ETHILON Nylon Suture recalled for defective needles

  Some ETHILON Nylon Suture needles have distorted curvature and may break during surgical use. This could cause additional injury to soft tissue or blood vessels, including tearing or bleeding during surgery.

• 2026-10-23FDA-FoodProsperity Organic Foods IncClass II
  Miyoko's Creamery plant milk butter recalled for contamination

  Miyoko's Creamery European Style Salted Plant Milk Butter (8 oz units, UPC 857554005773) has been recalled because some packages may contain yeast, mold, and E. coli. The affected product was distributed to Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Maryland, New Jersey, New Hampshire, and Wisconsin.

• 2026-10-23FDA-FoodEDEN BROTHERSClass I
  Eden Brothers Broccoli Seeds recalled for Salmonella risk

  Eden Brothers Broccoli Seeds (Calabrese variety) in 1 oz and 1 pound pouches may be contaminated with Salmonella. The affected product was packed in 2027 under lot numbers 1022067 and 1022068, and was distributed nationwide.

• 2026-10-23FDA-FoodFORTUNA MARKETING, INCClass I
  ZestiGreens Broccoli Seeds recalled for Salmonella risk

  ZestiGreens Broccoli Seeds for Sprouting & Microgreens (8 oz and 16 oz packages) may be contaminated with Salmonella. The seeds were primarily sold through Amazon. No illnesses have been reported.

• 2026-10-23FDA-FoodPink House Alchemy, LLCClass II
  Blue Bottle Coffee syrup recalled for mold contamination risk

  Blue Bottle Coffee 4oz Sweet Blossom Simple Syrup bottles may be contaminated with mold (Aspergillus niger). The syrup was made by Pink House Alchemy in Fayetteville, Arkansas. Affected bottles have specific batch codes and expiration dates ranging from April 2026 to May 2028.

• 2026-10-23FDA-DrugHikma Pharmaceuticals USA INC.Class II
  Hikma Abirtega recalled for tablet weight uniformity failure

  Hikma Pharmaceuticals is recalling Abirtega (abiraterone acetate) 250 mg tablets due to failed weight uniformity specifications. Lot 3047 (expiring July 2027) does not meet quality standards. The issue was identified during quality testing; no injuries have been reported.

• 2026-10-23FDA-DrugSafecor Health, LLCClass II
  Safecor Health metoclopramide tablets recalled for co-mingled contamination

  Safecor Health is recalling specific batches of metoclopramide 5 mg tablets manufactured for Teva Pharmaceuticals due to co-mingled tablets in the bottles. Co-mingling means tablets from different batches or products may have been mixed together. The affected lot is 3116509 with an expiry date of 07/31/2027.

• 2026-10-23FDA-DrugGlenmark Pharmaceuticals Inc., USAClass II
  Glenmark Abiraterone Acetate tablets recalled for labeling issue

  Glenmark Pharmaceuticals is recalling Abiraterone Acetate Tablets USP 500 mg in 60-count bottles due to a labeling defect. The affected lot (13250135, expiring 11/2027) was distributed nationwide. No injuries have been reported.

• 2026-10-23FDA-DrugThe Ritedose CorporationClass II
  Ritedose Formoterol Fumarate inhalation solution recalled for impurity concerns

  Ritedose Pharmaceuticals recalled one lot of Formoterol Fumarate Inhalation Solution (20mcg/2mL) because it failed quality testing for impurities and degradation. The affected lot (25BL0, expiring 02/28/2027) was distributed nationwide. No injuries have been reported.

• 2026-10-22FDA-PRWinCo Foods LLC
  WinCo Foods Hoagie Rolls recalled for undeclared sesame

  WinCo Foods Brand Hoagie Rolls with Best By dates between September 10 and November 3, 2026 contain sesame flour that is not listed on the package label or ingredient statement. People with a sesame allergy or sensitivity could have a serious allergic reaction if they eat this product. No illnesses have been reported so far.

• 2026-10-22FDA-PRNatural Grocers
  Natural Grocers mung beans recalled for glass fragments

  Natural Grocers Brand Organic 2-Pound Mung Beans may contain sharp glass fragments. The company received customer complaints about glass in the product and is recalling affected packages. No injuries have been reported so far.

• 2026-10-22FDA-DeviceAVID Medical, Inc.Class II2 products
  Halyard ANTERIOR HIP PACK recalled for non-sterile component

  Halyard ANTERIOR HIP PACK surgical kits (model SOAH31) contain a component that was not properly sterilized before packaging. The component was placed outside the sterile barrier and did not receive the required sterilization treatment. This affects 56 kits distributed in Arizona with lot number 1689215 and expiration date 11/06/2026.

• 2026-10-22FDA-DeviceMedline Industries, LPClass II13 products
  Medline C-section drape recalled for adhesive residue issue

  Medline Industries has recalled certain sterile surgical drapes used during cesarean sections because they can be difficult to remove from patients and may leave adhesive residue on the skin. The recall affects specific lot numbers distributed nationwide and internationally.

• 2026-10-22FDA-DeviceSolstice CorporationClass II
  Solstice Xact mole marker recalled for detaching material

  The radiopaque (X-ray visible) material on the Xact mole marker can detach during use. When this happens, the loose material may create artifacts (unwanted marks or shadows) on mammography images, potentially affecting image quality and interpretation.

• 2026-10-22FDA-DeviceMedtronic NeuromodulationClass II2 products
  Medtronic InterStim SureScan MRI Leads recalled for incompatibility risk

  Medtronic Neuromodulation has recalled certain InterStim SureScan MRI Leads (models 978A1 and 978B1 in lengths 28cm, 33cm, and 41cm) because of an error in component selection. If an incompatible lead or percutaneous extension is used during implantation, the system may not function properly and could require surgical replacement.

• 2026-10-22FDA-DeviceMedtronic MiniMed, Inc.Class II
  Medtronic MiniMed Go App recalled for failed dose reminders

  A software bug in MiniMed Go version 1.2.1 broke the long-acting insulin dose reminder feature for users who had it enabled in earlier versions. When users updated the app, the reminder stopped working silently—without any alert to the user. This could cause users to miss or delay insulin doses, or accidentally take a double dose if they're unsure whether they already dosed.

• 2026-10-22FDA-Devicerestor3d Inc.Class II
  restor3d MTP Implant recalled for non-sterile units

  Sixteen restor3d MTP foot implants were distributed without proper sterilization. The implants showed orange sterilization indicators, meaning they were never exposed to the sterilization process required to make them safe for surgery. These implants are used to treat arthritis and other conditions in the big toe joint.

• 2026-10-22FDA-DeviceBoston Scientific Cork, Ltd.Class II41 products
  Boston Scientific Direxion microcatheter recalled for defective coating

  Boston Scientific has recalled specific batches of Direxion Torqueable Microcatheters due to manufacturing defects. The hydrophilic coating on the tip of the catheters may not have been properly cured, and some nitinol sleeves have raised ridges from laser cutting misalignment. These defects could affect the device's performance during medical procedures.