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
34,960 found- Stop using nowConsumer product
John Deere Recalls Frontier Grooming Mowers Due to Entanglement Injury Hazard (Recall Alert)
John Deere recalls Frontier grooming mowers (FM3012, GM1060, etc.) due to incorrect assembly causing entanglement injuries. Consumers must stop using and contact a dealer for free repair.
John DeereSep 4, 2019 - Stop using nowConsumer product
Gator Utility Vehicles Recalled by John Deere Due to Crash Hazard (Recall Alert)
John Deere recalls XUV835 Gator utility vehicles with model number XUV835 printed on hood. Improper throttle cable routing can cause melting, leading to vehicle stalls and crash hazards. Affected owners must stop use and get free repairs.
John DeereSep 4, 2019 - Use cautionConsumer product
Artizen Oils Recalls Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements, Risk of Poisoning
Artizen Oils recalls wintergreen and birch essential oils bottles sold before April 2019 due to non-child-resistant packaging, posing poisoning risk to young children. Consumers should remove from reach and get free child-resistant caps.
Artizen OilsSep 4, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Achilles Express Bone Sonometer
GE Healthcare recalls Achilles Express Bone Sonometer models with European CEE-7/7 Type Power Cords that lack protective earth connection pins for countries requiring three protruding pins.
GE HealthcareSep 3, 2019 - Lower riskMedical device
Medtronic Vascular Galway DBA Medtronic Ireland recalls Solarice Rapid Exchange Balloon Dilatation Catheter, Product Numbers: SLC1506X, SLC1510X, SLC1512X, SLC1515X, SLC1520X,
Medtronic recalls Solarice Rapid Exchange Balloon Dilatation Catheters with specific product numbers due to a slightly larger stylette that may cause removal difficulties during medical procedures.
MedtronicSep 3, 2019 - UnratedDrug
Compounded Solutions in Pharmacy recalls 10% Acetyl-L-Cysteine Ophthalmic Solutions, dispensed in a) 5ml, b) 10ml c) 15 ml, dropper bottles
Recall of 10% Acetyl-L-Cysteine Ophthalmic Solutions in 5ml, 10ml, and 15ml dropper bottles due to lack of processing controls. Affected lots with specific expiration dates.
Compounded Solutions in PharmacySep 3, 2019 - Stop using nowDrug
Coast Quality Pharmacy, LLC dba Anazao Health recalls Hydromorphone HCL and Baclofen and Clonidine HCL in all strengths, all doses and all packaging, AnazaoHealth 5710
Anazao Health recalls specific lots of Hydromorphone HCL, Baclofen, and Clonidine HCL due to lack of processing controls and fungal contamination.
Anazao HealthSep 3, 2019 - Lower riskFood
Euroline Foods LLC recalls TAINY VOSTOKA DRY FRUIT MIX QUINCE COMPOTE 17.65oz (500 gram); Container code# 27032019; UPC code 4605932006203.
Euroline Foods recalls Tainy Vostoka Quince Compote due to undeclared sulfites. Consumers should check product codes to determine if affected.
Euroline FoodsSep 3, 2019 - Stop using nowConsumer product
The Beaufort Bonnet Company Recalls Handmade Knit Dolls Due to Injury Hazard
The Beaufort Bonnet Company is recalling handmade knit dolls due to a sewing needle in the stuffing that could cause puncture injuries. Affected dolls include animal-themed styles like Ellie Mae the Cat and Frat E. Fox. Consumers should stop using and get a gift card refund.
The Beaufort Bonnet CompanySep 3, 2019 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Air Bags
Subaru recalls 2014 Legacy vehicles with risk of passenger air bag inflator explosion causing serious injury or death. Owners must replace inflator free of charge.
SubaruSep 1, 2019 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Air Bags
Subaru is recalling 2014 Legacy vehicles with passenger air bag inflators that may explode during crashes, causing serious injury or death. Owners must have the inflator replaced free of charge by dealers.
SubaruSep 1, 2019 - Use cautionVehicle
SUBARU LEGACY (2014) recall — Air Bags
Subaru recalls 2014 Legacy vehicles with risk of air bag inflator explosion causing serious injury or death. Owners must replace the inflator free of charge.
SubaruSep 1, 2019 - Use cautionVehicle
LEXUS GX460 (2017) recall — Air Bags
Toyota is recalling 2017 Lexus GX460 vehicles with air bag inflators that may explode due to humidity and temperature exposure, risking serious injury or death. Owners should contact Toyota for replacement.
ToyotaSep 1, 2019 - Use cautionVehicle
FERRARI 488 GTB (2018) recall — Air Bags
Ferrari recalls 2018 488 GTB models with passenger air bags that may explode during crashes, causing serious injury or death. Owners must have the air bag assembly replaced free of charge.
FerrariSep 1, 2019 - Lower riskFood
UNFI General Corporate recalls Apetina Marinated Olives & Feta in Olive Oil, packed in 3.1 LB pals; 4 pals/case; UPC: 0009393605697
Apetina Marinated Olives & Feta in Olive Oil was recalled due to being held at room temperature instead of refrigerated, posing a food safety risk. Consumers should check UPC 0009393605697 for affected products.
ApetinaSep 1, 2019 - Lower riskMeat & poultry
American Beef Packers, Inc. Recalls Raw Beef Products Deemed Unfit for Human Consumption
USDA FSIS recalls 24,428 pounds of raw beef products deemed unfit for human consumption due to improper testing. Consumers are urged not to consume and should discard or return items.
American Beef PackersAug 31, 2019 - Use cautionMeat & poultry
Heatherfield Foods Inc. Recalls Pork Sausage Products Due to Misbranding
Heatherfield Foods recalls 4,380 pounds of gluten-free pork sausages that contain wheat, a common allergen, due to misbranding. Consumers are urged not to consume these products.
Heatherfield FoodsAug 30, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry
GE Healthcare recalls ApexPro Telemetry Server System units that may not provide visual or audible alarms for ECG arrhythmias, ECG leads failure, or pulse oximetry under certain conditions. Affected units have specific serial numbers listed in the recall notice.
GE HealthcareAug 30, 2019 - Lower riskMedical device
Pajunk GmbH recalls SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.
Pajunk recalls SPROTTE lumbar puncture needles with potential packaging issues affecting sterility. Affected models include 22G, 21G, 20G sizes in 25-count boxes. Contact for remedy details.
PajunkAug 30, 2019 - Use cautionMedical device
Spacelabs Healthcare, Inc. recalls Xhibit Central, Model No. 96102 - Product Usage: intended use is to provide clinicians with central monitoring of
Spacelabs Healthcare recalls Xhibit Central Model 96102 software versions 1.3.1-1.3.4 due to potential audio alarm loss after power failure or cable disconnection, which could delay recognizing patient emergencies.
Spacelabs HealthcareAug 30, 2019 - Use cautionMedical device
Philips Ultrasound Inc recalls Transducer S8-3t UDI (01)00884838073524 REF 989605431171 Can be used as accessory with: EPIQ 7, Affiniti 70, EPIQ 5,
Philips recalls S8-3t transducers for potential patient injury due to incorrect temperature measurement during transesophageal echocardiography (TEE) scans.
PhilipsAug 30, 2019 - UnratedDrug
Plastikon Healthcare LLC recalls Milk of Magnesia USP, 2400 mg/30 mL, Magnesium Hydroxide 2400 mg, 30 mL unit dose cups, For Institutional Use Only,
Plastikon Healthcare recalls institutional Milk of Magnesia USP 2400mg/30mL units due to microbial contamination. Products failed bioburden testing for aerobic bacteria. Affected lots: 19027D, 19027E (exp 07/21).
Plastikon HealthcareAug 30, 2019 - UnratedDrug
Pacifico National, Inc. dba AmEx Pharmacy recalls Bevacizumab, 2.5 mg/0.1 mL, Norm-Ject Syringe Intravitreal Injection, Single use only, Rx only, Repackaged by AmEx
AmEx Pharmacy recalls Bevacizumab 2.5 mg/0:1 mL syringes due to lack of sterility assurance. All remaining lots within expiry date are affected.
AmEx PharmacyAug 30, 2019 - Lower riskFood
Cena Vegan recalls Cena Vegan Pollo Asado Plant-Based Meat; Net Wt. 16 oz. (448 grams) retail, Net Wt. 5 lb. - food service; UPC: 8 55687
Cena Vegan recalls plant-based chicken meat products due to undetected soy protein allergen. Products sold between April 2020 and September 2020 with UPC 8 55687 00701 5 may contain hidden soy protein that could cause allergic reactions.
Cena VeganAug 30, 2019 - UnratedFood
Hiland Dairy Foods recalls One-Half Gallon Hiland Dairy Lemonade UPC: 72060-00519-6 packaged in plastic bottle and Pint Hiland Dairy Lemonade UPC:
Hiland Dairy Foods recalls half-gallon and pint lemonade products with undeclared milk. Consumers should check UPCs and sell dates for affected items.
Hiland Dairy FoodsAug 30, 2019 - Stop using nowFood
WESTON FOODS (CANADA) INC recalls Publix 8 inch T/S pumpkin pie US; 623g (22 oz. or 1 LB 6 oz.), Carton, 6 units per case
Weston Foods Canada recalls Publix pumpkin pies with lead and metal pieces. Consumers should stop using affected lots before expiration dates.
Weston FoodsAug 30, 2019 - Stop using nowFood
Danone Waters of America, Inc recalls YoCrunch VANILLA LOWFAT YOGURT WITH SNICKERS PIECES 4 - 4 oz (113g) - 16 oz (453g) 6 packaged or 4 cups per case. UPC
Danone recalls YoCrunch Vanilla Lowfat Yogurt with Snickers Pieces due to undeclared peanuts and eggs. Check your UPC and date code.
YoCrunchAug 30, 2019 - Lower riskFood
High Liner Foods Inc. recalls Sea Cuisine Citrus Herb Rubbed Salmon. Two Atlantic salmon fillets with lemon, herb, sea salt, and pepper; NET WT 8 OZ
High Liner Foods recalls two Atlantic salmon fillets with citrus herb rub for Listeria monocytogenes contamination. Consumers should check product codes and follow safety steps.
High Liner FoodsAug 30, 2019 - Use cautionFood
Diamond Crystal Brands Inc recalls Chef's Companion Instant Chocolate Mousse Mix Net Wt. 1 lb 14 oz (851 g), Dist by Diamond Crystal Brands, Inc.
Diamond Crystal Brands recalls Chef's Companion Instant Chocolate Mousse Mix due to undeclared soy. Check your pantry for this allergen risk.
Chef's CompanionAug 30, 2019 - Stop using nowConsumer product
RH Recalls Turkish Robes Due to Violation of Federal Flammability Standard
RH recalls Ultra-Soft Turkish Robes due to flammability risks. Stop using immediately and contact RH for a full refund if purchased between Aug 2018 and Mar 2019.
RHAug 30, 2019
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