Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,021 found- Lower riskMedical device
BMC Medical Co., Ltd. recalls BMC/REACTHEALTH Luna G3 APAP REF LG 3600
BMC Medical Co., Ltd. is a leading manufacturer of medical devices and equipment. Our products are designed to meet the highest standards of quality and safety.
BMC Medical Co., Ltd.Jul 15, 2026 - Lower riskFood
Prospector Popcorn, LLC recalls Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.
Prospector Popcorn recalls 1.5 oz Chocolate Mocha Gourmet Popcorn due to inaccurate carbohydrate and cholesterol declarations on the label.
Prospector PopcornJul 15, 2026 - Lower riskDrug
Asclemed USA Inc. recalls Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed
Asclemed recalls Lidolog Kit (2% Lidocaine injection) due to label wrap covering barcode, making scanning difficult. Affected units have specific lot and expiration dates.
AsclemedJul 15, 2026 - Use cautionVehicle
HYUNDAI KONA (2025) recall — Seat Belts
Hyundai recalls certain 2024-2025 Kona vehicles for rear seat belt buckle failure that may increase crash injury risk. Owners must stop using rear center seat until fixed.
HyundaiJul 15, 2026 - Use cautionVehicle
FORD EXPLORER (2025) recall — Seats
Ford is recalling 2020-2026 Explorer vehicles with second-row seat switches that may bind, causing seats to unlatch unexpectedly during crashes. Owners must have seats inspected by dealers for free replacement of the bezel.
FordJul 15, 2026 - Use cautionVehicle
FORD EXPLORER (2019) recall — Structure
Ford is recalling 2019 Explorer vehicles with roof rail covers that may detach, creating road hazards and crash risks. Owners should contact Ford for free repairs or replacements.
FordJul 14, 2026 - Stop using nowMedical device
AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE REF: KRIV26-02
AVID Medical recalls Halyard IV Start Kit (non-sterile) with contaminated Aspergillus penicillioides in applicators. Stop using to prevent infection risks.
AVID MedicalJul 14, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02
AVID Medical recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02 due to potential contamination from paper lidding wrinkles breaching seals. Affected units sold from 7/31/2026 with specific lot numbers.
AVID MedicalJul 14, 2026 - Lower riskMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls Citrasate, Liquid Acid Concentrate for Bicarbonate Hemodialysis: Product Numbers: 08-2251-CA, 08-3251-CA, 13-2251-CA;
Fresenius Medical Care recalls Citrasate Liquid Acid Concentrate for Bicarbonate Hemodialysis with product numbers 08-2251-CA, 08-3251-CA, and 13-2251-CA due to reported blue-green discoloration in the product.
Fresenius Medical CareJul 14, 2026 - Lower riskMedical device
ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture
ConMed recalls 5.5mm GENESYS CrossFT Suture Anchors with possible incorrect patient implant cards, risking wrong device identification. Affected units have specific reference numbers.
ConMedJul 14, 2026 - Use cautionMedical device
Boston Scientific Corporation recalls Suture Cinch Long 1pk. Endoscopic tissue approximation device.
Boston Scientific recalls Suture Cinch Long 1pk endoscopic tissue approximation devices that may fail to deploy the cinch implant or cut sutures as intended. Affected units have specific lot numbers and expiration dates.
Boston ScientificJul 14, 2026 - Use cautionMedical device
Hollister Ulc recalls Onli 17cm Hydrophilic Urethral Intermittent Catheter, labeled as: 1) 82081 Ch08-17 Onli Hydrophilic Urethral
Hollister recalls select lots of 17cm hydrophilic urethral catheters due to manufacturing defects that may cause genitourinary trauma or bleeding. Affected units include specific SKUs and lot numbers.
HollisterJul 14, 2026 - Lower riskMedical device
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY ,
Cardinal Health recalls 11 surgical kit types due to unexpected endotoxin variability in Medicom Ritmed Neurological Sponges, which could pose risks during procedures.
Cardinal HealthJul 14, 2026 - UnratedDrug
Precision Dose Inc. recalls Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080,
Precision Dose recalls Glycopyrrolate Oral Solution (1 mg/5 mL) due to failed impurities and degradation specifications. This prescription medication may pose risks if used as intended.
Precision DoseJul 14, 2026 - UnratedDrug
Rohto-Mentholatum (Vietnam) Co., Ltd. recalls Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0.012%, polysorbate 80 0.2%), Sterile, 0.4 FL OZ (13 mL)
Rohto recalls cooling eye drops due to lack of assurance of sterility. Products made in Vietnam with specific lot numbers and expiration dates are affected. Consumers should contact the manufacturer for details.
RohtoJul 14, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Medtronic recalls MiniMed 670G insulin pumps with specific model numbers due to potential cleaning issues causing insulin delivery errors. Affected users should contact Medtronic for details.
Medtr: MiniMedJul 13, 2026 - Lower riskMedical device
Siemens Healthcare Diagnostics Products Ltd. recalls Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen REF(s):L2kSY2/10489085; L2KSY6/10488319 IVD, RxOnly
Siemens Healthineers recalls Immulite 2000 Syphilis Screen systems that may report false negatives for syphilis tests, risking undetected infections. Affected units include specific lot codes and reference numbers.
Siemens HealthineersJul 13, 2026 - Lower riskMedical device
Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200
Kico recalls ARVIS Surgical Navigation System Gen 2 (model IN-29200) due to potential image tilt in eyepiece. This may affect surgical alignment accuracy during procedures like knee or hip replacements.
KicoJul 13, 2026 - Lower riskMedical device
Gentherm Medical, LLC recalls Blanketrol II Model 222S; Thermal regulating system.
Gentherm recalls Blanketrol II Model 222S thermal regulators due to overheating risk causing shutdowns. Affected units have specific serial numbers.
GenthermJul 13, 2026 - Use cautionMedical device
Siemens Healthcare Diagnostics, Inc. recalls Beckman Coulter, Emit 2000 Quinidine Assay REF: OSR4Q229 Contents: R1: 2 x 23 mL;R2 2x13 mL
Beckman Coulter recalls Emit 2000 Quinidine Assay kits with specific lot numbers due to potential for inaccurate quinidine measurements, risking suboptimal patient treatment and possible life-threatening cardiac issues.
Beckman CoulterJul 13, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU
Medline recalls neonatal breathing circuits with potential sporadic failure causing infant respiratory issues. Affected models include HUD78007, HUD78009, and others. Stop using immediately if you have these circuits.
MedlineJul 13, 2026 - Use cautionFood
KHONG GUAN (HQ) recalls BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC:
KHONG GUAN recalls 14.1 oz glutinous rice balls with black sesame filling due to undeclared peanuts. Consumers should check UPC 6908791000084 for affected products.
KHONG GUANJul 13, 2026 - Lower riskMedical device
OBP Medical Corporation recalls OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
OBP Medical recalls X-Small ER-Spec vaginal speculums with LED light due to potential burr on plastic blade that could cause sharp edges for patient or provider.
OBP MedicalJul 13, 2026 - Lower riskMedical device
Straumann USA LLC recalls GM Helix Implant, Endosseous Dental Implant Article No. 109.984
Straumann recalls GM Helix dental implants with possible packaging mismatch. Incorrect implants could cause bone compression during installation if bone volume is sufficient.
StraumannJul 13, 2026 - Stop using nowFood
PT Organics Limited recalls Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720.
PT Organics recalls specific lots of 4oz banana and strawberry fruit puree pouches due to possible thin, soft plastic strands.
PT OrganicsJul 13, 2026 - Use cautionDrug
Rising Pharma Holding, Inc. recalls Rising, Cyproheptadine Hydrochloride Syrup, 2mg/5 mL, 473 mL (ONE PINT), Rx only, Manufactured for: Rising Pharma
Rising Pharma recalls Cyproheptadine Hydrochloride Syrup (2mg/5 mL) due to precipitate formation. Check your bottle's lot number and expiration date for affected batches.
Rising PharmaJul 13, 2026 - Lower riskDrug
Major Pharmaceuticals recalls Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only,
Major Pharmaceuticals recalls 50 mcg levothyroxine tablets due to subpotent drug levels. This may cause inadequate thyroid hormone replacement. Consumers should contact the manufacturer for details.
Major PharmaceuticalsJul 13, 2026 - Use cautionFood
SLT Foods Inc. recalls Khazana The Treasure Spice Magic Fennel Candy, 5 lbs., Poly Plastic Bag, 4 per case
SLT Foods recalls Khazana Spice Magic Fennel Candy due to undeclared Yellow 5 & 6, Red 3, and Blue 1. Check your product details.
KhazanaJul 10, 2026 - Use cautionVehicle
GRAND DESIGN LINEAGE (2026) recall — Equipment
Grand Design is recalling certain 2026-2027 Lineage RVs with MaxxAir N-Series Maxxfan fans due to overheating printed circuit boards that could cause fire. Owners received letters July 21, 2026.
Grand DesignJul 10, 2026 - Lower riskMedical device
Paragon 28, Inc. recalls Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; foot implant
Paragon 28 recalls a specific foot implant model due to elevated oxygen levels potentially reducing material strength. Affected units include Lot AOCIA6123.
Paragon 28Jul 10, 2026
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83,609 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.