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
35,025 found- Lower riskMedical device
Ethicon, Inc. recalls Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to hold closed easily approximated skin edges of
Ethicon recalls Dermabond Advanced Topical Skin Adhesive due to potential sterility breach from red packaging tape. Affected units have specific product codes and expiration dates.
EthiconJan 4, 2021 - Lower riskMedical device
Aomori Olympus Co., Ltd. recalls INJECTOR FORCEMAX 25G 2.5MM, model no. NM-400U-0425 - Product Usage: Used with endoscopes to perform endoscopic
Olympus recalls INJECTOR FORCEMAX 25G 2.5MM (model NM-400U-0425) due to potential inadequate sterile packaging seals. Patients could develop infections if non-sterile equipment is used. Affected units were sold in specific batches.
OlympusJan 4, 2021 - Lower riskDrug
Nostrum Laboratories Inc recalls Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg, 100 tablets per bottle, Rx Only, Manufactured by:
Nostrum Laboratories recalls 750mg Metformin Hydrochloride Extended-Release Tablets due to N-Nitrosodimethylamine (NDMA) impurity exceeding safe levels. Rx-only medication sold in 100-tablet bottles with NDC 29033-056-01.
Nostrum LaboratoriesJan 4, 2021 - Lower riskFood
Ittella International, LLC recalls Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 850015982569
Tattooed Chef recalls plant-based sausage breakfast bowls with a gluten-free claim on the lid despite containing wheat flour and other allergens. Consumers should check for the specific lot codes and contact the company for details.
Tattooed ChefJan 4, 2021 - Use cautionVehicle
HYUNDAI IONIQ ELECTRIC (2020) recall — Electrical System
Hyundai recalls 2020 Ioniq Electric vehicles with potential lithium-ion battery short-circuit risk. Owners must park outside and follow battery update steps to prevent fire.
HyundaiJan 3, 2021 - Use cautionMeat & poultry
Courage Production, LLC. Recalls Ready-to-Eat, Fully Cooked Polish Sausage Products due to Misbranding and an Undeclared Allergen
USDA recalls 1,645 pounds of ready-to-eat Polish sausages from Courage Production that contain undeclared mozzarella cheese, a known allergen. Consumers are urged not to consume these products.
Courage ProductionJan 2, 2021 - Use cautionVehicle
VOLKSWAGEN JETTA (2021) recall — Seats
Volkswagen recalls 2021 Jetta vehicles with missing front seat bolts that could move during crashes, increasing injury risk. Owners must have seats inspected by dealers for free.
VolkswagenJan 2, 2021 - Use cautionVehicle
RAM 1500 (2021) recall — Service Brakes, Hydraulic
Chrysler recalls 2020-2021 RAM 1500 Classic SLT trucks with brake pedal separation risk. Owners must not drive until inspected and repaired by dealers.
ChryslerJan 2, 2021 - UnratedDrug
Precision Dose Inc. recalls Chlorhexidine Gluconate Oral Rinse USP 0.12%, packaged in a) 15 mL x 30 Unit Dose Cups (30-pack case) NDC 68094-028-61,
Precision Dose Inc. recalls 0.12% Chlorhexidine Gluconate Oral Rinse due to cGMP deviations. Products sold in 30-pack and 100-pack cases with specific lot numbers from 2021-2022.
Precision DoseJan 1, 2021 - Lower riskMeat & poultry
FSIS Issues Public Health Alert for Frozen, Fully Cooked, Not Shelf Stable Chicken Sriracha Ravioli Products Due to Misbranding and an Undeclared Allergen
FSIS public health alert: 49 pounds of frozen chicken sriracha ravioli may contain undeclared soy allergen. Consumers with soy allergies should not consume these products.
Fresh Thyme Farmers MarketDec 31, 2020 - UnratedFood
Rhino Foods, Inc. recalls AF01886 NTFA No egg Ready-to-Eat Chocolate Chip Cookie Dough Dough- 20 lb. sold frozen
Rhino Foods recalls 20lb frozen chocolate chip cookie dough dough with possible Listeria monocytogenes contamination. Consumers should check expiration dates and contact for details.
Rhino FoodsDec 31, 2020 - Stop using nowConsumer product
Anticimex Recalls SMART Connect Mini Devices Due to Fire and Injury Hazards (Recall Alert)
Anticimex recalls SMART Connect Mini Devices due to fire and injury risks from overheating power supplies. Consumers must stop using immediately and contact Anticimex for removal.
AnticimexDec 31, 2020 - Lower riskMedical device
Beckman Coulter Inc. recalls ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems
Beckman Coulter recalls ACCESS SARS-CoV-2 IgG QC cards with label errors for standard deviation values. This may affect test accuracy in some lab settings.
Beckman CoulterDec 30, 2020 - Lower riskMedical device
Baxter Healthcare Corporation recalls Gambro Cartridge Blood Transport System for Hemodialysis Blood Set, product code 109536 - Product Usage: intended for
Baxter recalls Gambro Cartridge Blood Transport System for hemodialysis blood sets due to kinked access lines observed during treatment. Affected units may cause treatment complications.
BaxterDec 30, 2020 - Lower riskDrug
AuroMedics Pharma LLC recalls Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose Vial, For Intravenous Use Only, Distributed
AuroMedics Pharma recalls 100mL IV acetaminophen injection vials with discoloration or failed pH tests. These vials may not be safe for medical use. Check your vials for discoloration or unusual pH levels.
AuroMedicsDec 30, 2020 - Lower riskDrug
Allergan, PLC. recalls Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie
Allergan recalls Refresh Relieva PF Preservative-Free Lubricant Eye Drops due to missing instructions for use. Consumers should check product labels for lot numbers and expiration dates.
AllerganDec 30, 2020 - Lower riskFood
Ocean Providence Minneapolis LLC recalls Frozen Ground Tuna, Wild Caught, Production Date: 06/01/2020. Product of Vietnam, Net Wt: 11 lbs. x 2: 22 lbs. Imported
Ocean Providence recalls 22-lb frozen wild-caught tuna from Vietnam produced June 1, 2020, due to potential histamine levels. Consumers should check product date and disposal if concerned.
Ocean ProvidenceDec 30, 2020 - Stop using nowConsumer product
Target Recalls Infant-Toddler Girl's One-Piece Rashguard Swimsuits Due to Choking Hazard
Target recalls Cat & Jack infant-toddler one-piece rashguard swimsuits with detachable snaps that can cause choking or lacerations. Consumers should return suits for full refunds.
Cat & JackDec 30, 2020 - Stop using nowConsumer product
Target Recalls Infant Rompers Due to Choking Hazard
Target recalls Cloud Island infant rompers due to snaps that can break or detach, posing choking and laceration risks to young children. Return for full refund at any Target store or use Target.com prepaid label.
Cloud IslandDec 30, 2020 - Lower riskMedical device
Allergan PLC recalls REFRESH CONTACTS¿ Contact Lens Comfort Drops 0.4 fl oz (12 mL) Sterile
Allergan recalls REFRESH Contact Lens Comfort Drops 0.4 fl oz due to missing instruction manual. Consumers should check product details and contact Allergan for guidance.
AllerganDec 29, 2020 - Stop using nowFood
Puratos Corporation recalls Tegral Satin EC CL Vegan Cake packaged in 50lbs bags
Puratos Corporation is recalling Tegral Satin EC CL Vegan Cake in 50lb bags due to undeclared milk and egg allergens. Check your product now.
PuratosDec 29, 2020 - Lower riskFood
Port City Bakery, Inc recalls AK 10 5/8" Par Baked Stuffed Crust, frozen Pizza Crust, Item 1115660, Case Count / Unit Weight, 283 Count / 21.5 oz.
Port City Bakery recalls frozen pizza crusts that may contain glass. Consumers should check product codes and contact the company for details.
Port City BakeryDec 29, 2020 - Lower riskFood
Avalanche Distributing, LLC recalls Valanga Gourmet brand Snickerdoodle Cookie with cinnamon sugar on the outside. Each cookie is wrapped and sold
Valanga Gourmet recalls Snickerdoodle cookies with cinnamon sugar due to unlisted milk in margarine. Check UPC 814524616004 for affected items. No remedy specified in recall.
Valanga GourmetDec 29, 2020 - Lower riskFood
Divvies LLC recalls "Divvies Vegan and Nut Free Vanilla Cupcakes with Vanilla Frosting ***Net. Wt. 6 oz. "
Divvies LLC recalls vegan cupcakes with undeclared milk and egg due to supplier ingredients. Consumers should check for specific lot numbers on the container.
DivviesDec 29, 2020 - Use cautionVehicle
YAMAHA FJR1300 (2018) recall — Power Train
Yamaha recalls 2016-2020 FJR13A/FJR13AE motorcycles due to potential transmission gear cracking under high speed, risking loss of control and crashes. Owners must have repairs done by dealers before riding.
YamahaDec 28, 2020 - Use cautionVehicle
YAMAHA XV1900 (2020) recall — Exterior Lighting
Yamaha recalls 2020 XV1900 motorcycles with front brake switch failure causing brake lights to stay on or cruise control to shut off unexpectedly, increasing crash risk. Owners must have repair completed before riding.
YamahaDec 28, 2020 - Use cautionMedical device
New Standard Device Inc recalls Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill
New Standard Device Inc recalls Metalogix Self-Drill Half-Pins due to reported tip breakages during surgery. Affected models include 5x30x215mm, 5x40x215mm, 5x60x215mm, and 5x80x215mm with specific lot numbers.
Metalogix Self-DrillDec 28, 2020 - Lower riskMedical device
Baxter Healthcare Corporation recalls FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable
Baxter recalls 5-size Flow Coupler Monitor devices with potential battery recharge issues. Affected units have specific serial numbers and sizes. No remedy stated in recall.
BaxterDec 28, 2020 - Use cautionMedical device
Mar-Med Co recalls Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The device is
Mar-Med Co recalls Tourni-Cot Universal Tourniquets (Model TCU) due to risk of finger/toe injury if improperly removed. The device may tear and constrict blood vessels, causing tissue damage. Affected units have UDI 00855364004085.
Mar-Med CoDec 28, 2020 - Lower riskDrug
Akorn, Inc. recalls Levetiracetam Oral Solution, 100 mg/mL, 16 fl oz (473 mL) bottle, Rx Only, HI-TECH PHARMACAL CO., INC., Amityville, NY
Akorn recalls Levetiracetam Oral Solution bottles that leak. This medication is prescription-only and may cause spills if the container is defective.
AkornDec 28, 2020
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