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
35,004 found- Lower riskMedical device
Steris Corporation recalls Eagle 3000 Sterilizer, small steam sterilizer. Product Usage: The Eagle 3000 Small Sterilizer is designed for
Steris recalls Eagle 3000 Small Sterilizers with potential incorrect pressure safety valve in Preventive Maintenance kits. Affected units have specific serial numbers listed in the recall notice.
SterisOct 22, 2019 - Lower riskMedical device
Biomerieux Inc recalls BIOMERIEUX VIDAS 3, Compact immunoanalyzer with full traceability and automation
Biomerieux recalls VIDAS 3 compact immunoanalyzer with software versions 1.2+ due to expired calibration causing false test results. Affected units may need recalibration.
BiomerieuxOct 22, 2019 - Lower riskMedical device
Encore Medical, LP recalls EMPOWR Acetabular System, Non-Sterile, Model Numbers 803-15-023 803-15-026 803-15-027 803-15-028 803-15-029 803-15-030
Encore Medical recalls EMPOWR Acetabular System models 803-15-023 to 803-15-030 due to fracturing impactor balls that could cause joint debris. Affected patients should contact manufacturer for details.
Encore MedicalOct 22, 2019 - Use cautionMedical device
Edwards Lifesciences, LLC recalls EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in
Edwards Lifesciences recalls specific EZ Glide aortic cannula models due to potential separation during cardiopulmonary bypass, risking significant blood loss. Affected units have unique identifiers and lot numbers.
Edwards LifesciencesOct 22, 2019 - Use cautionMedical device
Steris Corporation recalls Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer, Steam
Steris recalls Evolution Loading Car and Transfer Carriage accessories for steam sterilizers due to potential front wheel locking failure causing unexpected forward falls.
SterisOct 22, 2019 - Lower riskDrug
Apotex Inc. recalls Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario
Apotex recalls 1,000-count Atorvastatin 40mg tablets due to foreign pravastatin tablets found in some bottles. This is a prescription-only medication.
ApotexOct 22, 2019 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Estradiol Vaginal Inserts USP, 10 mcg, packaged in a) 8-count Vaginal Inserts (with disposable applicators) per carton
Glenmark Pharmaceuticals recalls Estradiol Vaginal Inserts (10 mcg) due to difficulty pushing the plunger of the applicator. This is a drug recall for Rx-only products with specific batch numbers and NDC codes.
GlenmarkOct 22, 2019 - UnratedDrug
Sanofi-Aventis U.S. LLC recalls Cool Mint Tablets Maximum Strength Zantac 150 mg Sanofi Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219,
Sanofi recalls Cool Mint Zantac 150mg tablets due to detected NDMA impurity. Affected products include specific NDC codes and all lots. Consumers should check their product labels and contact Sanofi for details.
SanofiOct 22, 2019 - Stop using nowDrug
Green Lumber Holdings, LLC recalls Green Lumber Natural Fuel For Men capsule, packaged in packs of 2, 4 and 10 capsules, 2618 San Miguel Drive, Suite
Green Lumber Holdings recalls Natural Fuel For Men capsules due to undeclared Tadalafil. Check lot numbers XC12, XC06, XC10, XC02, XC04 for expiration dates through 2022.
Green LumberOct 22, 2019 - Stop using nowConsumer product
Federal Cartridge Recalls Blackhawk Gun Holsters Due to Injury Hazard
Blackhawk T-Series L2:2101213 gun holsters recalled due to safety switch malfunction causing unexpected firearm discharge. Consumers must stop using and get refunds.
BlackhawkOct 22, 2019 - Use cautionVehicle
AIRSTREAM BASECAMP (2020) recall — Trailer Hitches
Airstream recalls 2020 Basecamp trailers with potentially detachable trailer hitches that could cause crashes. Owners must contact Airstream for a free fix.
AirstreamOct 21, 2019 - Use cautionMedical device
Haemonetics Corporation recalls JAPAN CELL SAVER ELITE SET - 225ML - Product Usage: its related accessory components are intended for use to recover
Haemonetics recalls Japan Cell Saver Elite Set (225ml) due to potential leaks from bowl cracks causing device errors. Affected units include specific lots manufactured between Oct 2014 and Oct 2019.
HaemoneticsOct 21, 2019 - Lower riskMedical device
Beckman Coulter Inc. recalls MicroScan WalkAway-40 plus Instrument REF B1018-283
Beckman Coulter recalls MicroScan WalkAway-40 Plus instruments with incorrect 1-ampere power connector that may cause electrical issues. Affected units have specific serial numbers and model codes.
Beckman CoulterOct 21, 2019 - Lower riskMedical device
Integra LifeSciences Corp. recalls C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System
Integra recalls C7000 Clarity Ultrasonic Tissue Ablation System due to 30-minute drying cycle not meeting required 40-minute dry time for sterilization trays, risking incomplete sterilization.
Integra LifeSciencesOct 21, 2019 - Lower riskMedical device
Boston Scientific Corporation recalls Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 12cm UPN: M00536700
Boston Scientific recalls Advanix Pancreatic Stent models with incorrect 36-month shelf life label instead of approved 18-month. Affected units sold between Sep 2017 and Sep 2019. No immediate action needed but check for specific lot numbers.
Boston ScientificOct 21, 2019 - Lower riskMedical device
Cook Inc. recalls Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system,
Cook recalls Torcon NB Advantage Catheters due to potential sterility compromise from undersealed packaging. Affected units may cause infection if used. Contact Cook for details.
CookOct 21, 2019 - Lower riskDrug
Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center recalls PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL
Nephron recalls 5x10mL PF-Succinylcholine Chloride Injection due to incorrect or missing lot and expiration dates. This affects prescription-only injectable medication.
NephronOct 21, 2019 - UnratedFood
Riba Foods Inc recalls Fire Roasted Medium Arriba! Bacon Salsa with Real Bacon NET WT 16 OZ. UPC Code: 033907 20513 1 packaged in a clear
Riba Foods recalls Fire Roasted Medium Arriba! Bacon Salsa with Real Bacon (16 oz) because it contains undeclared milk. This product was sold with UPC 033907 20513 1 and best by date 02 SEP 21.
Riba FoodsOct 21, 2019 - Use cautionFood
T & R Enterprises USA, Inc. recalls Crab Rangoon 1.0 oz.
T & R Enterprises USA, Inc. recalls 1.0 oz. Crab Rangoon produced between 080119 and 092619 due to insanitary packaging conditions.
T & R EnterprisesOct 21, 2019 - Stop using nowMeat & poultry
George's Prepared Foods Recalls Ready-To-Eat Pork and Turkey Products due to Possible Salmonella Contamination
Great Value fully cooked pork and turkey sausage patties are recalled due to possible Salmonella contamination. Check your use-by dates and lot codes immediately.
Great ValueOct 18, 2019 - Use cautionMeat & poultry
Pride of Florida Recalls Beef Products due to Possible E. Coli O157:H7 Contamination
Pride of Florida is recalling approximately 64,797 pounds of raw beef products that may be contaminated with E. coli O157:H7. Consumers should throw away or return these products to the place of origin.
Pride of FloridaOct 18, 2019 - Use cautionMeat & poultry
T & R Enterprise USA Inc. Recalls Meat and Poultry Products Due to Insanitary Conditions
USDA FSIS recalls 126,000 pounds of meat and poultry egg rolls produced between August and September 2019 with insanitary conditions. Consumers urged not to consume and dispose of products.
T & R EnterpriseOct 18, 2019 - Use cautionMeat & poultry
MawMaw's Chicken Pies Recalls Chicken and Meat Products Due to Misbranding and Undeclared Allergens
USDA recalls MawMaw's Chicken Pies products due to milk and soy allergens not declared on labels. Consumers should stop using these items immediately.
MawMaw's Chicken PiesOct 18, 2019 - Use cautionVehicle
SUBARU IMPREZA (2019) recall — Electrical System
Subaru is recalling 2019 Impreza vehicles with electrical system issues that could cause stalling and crashes if a short circuit occurs while driving.
SubaruOct 18, 2019 - Use cautionVehicle
POLARIS SLINGSHOT (2019) recall — Electrical System
Polaris recalls 2015-2019 Slingshot motorcycles with damaged electrical terminals that could cause loss of lighting or gauges, increasing crash risk. Owners must have terminals inspected and fuses relocated free by dealers.
PolarisOct 18, 2019 - Lower riskMedical device
Capso Vision, Inc. recalls CapsoCAM Plus, UDI: 00867770000209
Capso Vision recalls specific CapsoCAM Plus capsule endoscopy systems with serial numbers starting with A017NP.699. A defect in the capsule window may crack when ingested, risking fluid leakage and data loss. Patients may need to repeat the exam.
CapsoOct 18, 2019 - Lower riskMedical device
Taewoong Medical Co., Ltd. recalls Niti-S Esophageal Stent, REF ES1806F, ES1808F, ES1810F, ES1815F, ES2006B, ES2010B, ES1612B, ES1615B, ES1810B, ES1812B,
Taewoong Medical recalls Niti-S esophageal stents with misprinted instructions that could lead to improper use. Affected models include ES1806F through ES2010B and specific serial numbers. Consumers should check their product details.
Taewoong MedicalOct 18, 2019 - Lower riskMedical device
Tornier, Inc recalls Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475 DWF601B 3700386944482 DWF601C 3700386944499
Tornier recalls Aequalis Ascend Flex humeral stems with specific part numbers due to potential movement in shipping packaging that could transfer PETG material to the stem.
TornierOct 18, 2019 - UnratedMedical device
Basic Reset Inc. recalls Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)
Basic Reset Energy FX products (Aluminum 100-3A and sleek 100-3B) were recalled by FDA due to being misbranded medical devices. All units sold between Nov 2017 and Sep 2019 are affected.
Basic ResetOct 18, 2019 - Lower riskMedical device
Brasseler USA I Lp recalls BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm, Total Length 112mm, Effective Length, 86mm - Product
Brasseler recalls 3.5mm twist drills with incorrect 2.5mm laser etching that could lead to improper surgical use. Affected units have lot number NR1VM.
BrasselerOct 18, 2019
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.