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 riskFood
McCormick & Company - MSS - HQ recalls Frank s Red Hot Buffalo Ranch Seasoning 153g, Plastic Bottles, 36 packages per case
McCormick recalls 36 packages of Frank s Red Hot Buffalo Ranch Seasoning due to possible Salmonella contamination. Consumers should check UPC 066200021047 for affected items.
McCormickJul 26, 2021 - Lower riskMeat & poultry
Top Notch Jerky LLC. Recalls Beef Jerky Products Due to Misbranding and Undeclared Allergens
Top Notch Jerky LLC recalls beef jerky products sold at PGA events due to undeclared anchovies, a known allergen. No injuries reported.
Top Notch JerkyJul 24, 2021 - Use cautionVehicle
MCLAREN 720S (2019) recall — Service Brakes, Hydraulic
McLaren is recalling 2019 720S vehicles with potential brake failure causing pulling during braking. Owners must have brakes inspected and repaired free by dealers.
McLarenJul 23, 2021 - Use cautionVehicle
CHEVROLET BOLT EV (2019) recall — Electrical System
GM recalls 2019 Chevrolet Bolt EVs with high voltage battery that could catch fire when fully charged. Owners must limit charge to 90% and avoid indoor overnight charging to reduce fire risk.
Chevrolet Bolt EVJul 23, 2021 - Lower riskMedical device
Mivi Neuroscience Inc recalls MIVI Super 90 8F Guide Catheter, 95 cm, REF MIA-9095S-IDE, For Investigational Use Only; sterile, and Super 90 8F Guide
Mivi Neuroscience recalls Super 90 8F Guide Catheters with possible pouch seal defects that could lead to nonsterility. Affected units include specific model numbers and expiration dates.
Mivi NeuroscienceJul 23, 2021 - Lower riskMedical device
Merge Healthcare, Inc. recalls Merge Hemo, Software packages 10.2, 10.3, and 10.4
Merge Healthcare recalls software versions 10.2, 10.3, and 10.4 due to safety issues when used with HL7 lab interfaces. Affected users should contact the company for updates.
Merge HealthcareJul 23, 2021 - Lower riskMedical device
BioMimetic Therapeutics, LLC recalls AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
BioMimetic Therapeutics recalls AUGMENT Injectable Kit (Model K30003010, Lot 1706343) due to incorrect vial tray packaging. This may cause improper use during injections.
BioMimetic TherapeuticsJul 23, 2021 - Use cautionMedical device
Boston Scientific Corporation recalls TheraSphere Administration Set, REF OTT-SPE-FP-226 (990226.SPE)
Boston Scientific recalls TheraSphere Administration Set model 990226.SPE due to potential leaks and loosening at patient catheter connection. Affected units include specific lot numbers and GTIN.
Boston ScientificJul 23, 2021 - Lower riskMedical device
Aspen Surgical Products, Inc. recalls Norton Arm Kit, Product Code 711400, (previous product code 031001), Sample Kit S711400
Aspen Surgical Products recalls Norton Arm Kits (product code 711400) manufactured between July 2019 and July 2021 due to potential sterilization failure increasing surgical infection risk.
Aspen Surgical ProductsJul 23, 2021 - Lower riskDrug
Professional Disposables International, Inc recalls PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick, (1's), Step 1, packaged as a) Step 1 Scrub, 1 Swabstick, NDC
Professional Disposables International recalls PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabsticks due to subpotent quality. This means the product may not contain enough active ingredient for intended use. Consumers should contact the manufacturer for details.
PDIJul 23, 2021 - Use cautionVehicle
HEARTLAND MALLARD (2021) recall — Equipment
Heartland is recalling 2021 Mallard trailers due to improper vent routing causing overheating and fire risk, plus carbon monoxide poisoning. Owners should contact customer service for free repairs.
HeartlandJul 22, 2021 - Lower riskMedical device
Becton, Dickinson and Company, BD Biosciences recalls BD" Mouse IgG2a Isotype Control APC X39 ASR
BD Biosciences recalls Mouse IgG2a Isotype Control APC X39 ASR due to potential false positive staining from contamination. Affected units have catalog number 340757 and lot number 0253432.
BD BiosciencesJul 22, 2021 - Use cautionMedical device
Philips Ultrasound Inc recalls EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Philips recalls EPIQ Elite and other ultrasound systems due to swivel lock failure that may cause musculoskeletal injuries during patient or user movement.
PhilipsJul 22, 2021 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter prismaflex, HF 1000 PAES membrane, REF 107140 Used with Prismaflex or PrisMax control units for continuous fluid
Baxter recalls Prismaflex HF 1000 PAES membrane (lot 20B2330M) due to potential unsterilized products affecting medical treatments. Affected users should contact Baxter for guidance.
BaxterJul 22, 2021 - Lower riskFood
Hiland Dairy Foods Company LLC recalls Hiland 100% Pure Apple Juice From Concentrate No Sugar Added Pasteurized 4 FL OZ (118 mL) packaged in paper cartons 75
Hiland Dairy Foods recalls 100% pure apple juice with elevated inorganic arsenic levels. Products sold between July 2021 and August 2021 in paper cartons.
HilandJul 22, 2021 - Stop using nowConsumer product
Polaris Recalls RZR Recreational Off-Road Vehicles Due to Fire Hazard (Recall Alert)
Polaris recalls 2021 RZR Pro XP and Pro XP 4 off-road vehicles due to a fire risk from oil leaks caused by turbocharger casting defects. Owners must stop using and get repairs.
PolarisJul 22, 2021 - Stop using nowConsumer product
Polaris Recalls GENERAL Recreational Off-Highway Vehicles Due to Crash Hazard (Recall Alert)
Polaris recalls 2021 General 1000, 4 1000, XP 1000 and XP 4 1000 off-highway vehicles due to brake pedal pivot bracket weld separation causing loss of brake function.
PolarisJul 22, 2021 - Stop using nowConsumer product
BRP Recalls Side-by-Side Vehicles Due to Fire Hazard (Recall Alert)
BRP recalls 2020-2021 Defender HD10 side-by-side vehicles with track kits due to snow obstruction causing overheating and fire risk. Owners must stop using in snow and contact a dealer for repair.
BRPJul 22, 2021 - Stop using nowConsumer product
Bel Furniture Recalls Barrington 5-Drawer Chests Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Bel Furniture (Recall Alert)
Bel Furniture recalls Barrington 5-Drawer Chests due to unstable design that can tip over, causing entrapment and serious injury to children. Consumers must stop using and return for refund or installation of tip-over restraints.
Bel FurnitureJul 22, 2021 - Use cautionVehicle
NISSAN ROGUE SPORT (2021) recall — Seat Belts
Nissan recalls 2021 Rogue Sport vehicles with seat belt retractors that may deactivate early, risking child seat safety during crashes. Owners must have seat belts replaced free by dealers.
NissanJul 21, 2021 - Use cautionVehicle
BMW 330E (2021) recall — Seat Belts
BMW recalls certain 2021 330e models due to seat belt retractors that may deactivate early in crashes, increasing injury risk. Dealers will replace faulty parts free of charge.
BMWJul 21, 2021 - Use cautionVehicle
BENTLEY CONTINENTAL GT (2021) recall — Seats
Bentley recalls 2020-2021 Continental GT vehicles where rear passengers may get trapped by front seats during movement, increasing injury risk. Owners must update software for free.
BentleyJul 21, 2021 - Lower riskMedical device
Cardiovascular Systems Inc recalls DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM, 1.5MM SOLID, 145 CM, REF DBP-150SOLID145
Cardiovascular Systems recalls DIAMONDBACK 360 GEN2 peripheral orbital atherectomy systems due to potential mislabeling of crown sizes, which could lead to incorrect use in medical procedures.
Cardiovascular SystemsJul 21, 2021 - Lower riskMedical device
Merit Medical Systems, Inc. recalls MERITMEDICAL Prelude Short Sheath Introducer, REF: PSS-6F-4-018MT, 21G 6F(2.0 mm) 4 cm, Max Guide Wire 0.018" (0.46
Merit Medical recalls Prelude Short Sheath Introducer (REF: PSS-6F-4-018MT) due to potential incorrect dilator in package. This may cause complications during medical procedures. Affected units were sold with specific model and lot numbers.
Merit MedicalJul 21, 2021 - Use cautionMedical device
Beckman Coulter Inc. recalls DxA 5000 (DxA Automation System, DxA 5000 fit), "For in Vitro Diagnostic Use", Reference Numbers: B87352 with B57634,
Beckman Coulter recalls DxA 5000 devices with specific serial numbers due to potential sample contamination and infection risks. Affected units may cause delays in medical treatment and blood-borne pathogen exposure.
Beckman CoulterJul 21, 2021 - Lower riskMedical device
Trophy SAS recalls CS¿9600¿is¿an¿extraoral¿system¿intended¿to¿produce¿two-dimensional¿and¿three-dimensional¿digital¿X-ray¿images¿of¿the¿den
Trophy SAS recalls CS9600 extraoral X-ray systems that may fail to function as intended, affecting dental and medical imaging for pediatric and adult patients.
Trophy SASJul 21, 2021 - Lower riskMedical device
Cordis Corporation recalls Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Cordis recalls 5F Universal Flush F4 Super Torque MB Angiographic Catheters (REF SRD6785MB) due to potential entrapment between devices and vessel walls, risking marker band dislodgement.
CordisJul 21, 2021 - Use cautionMedical device
Implant Resource Inc recalls MPR Slotted Mallet, labeling etched onto devices as follows: Medical Products Resource 800.524.5194 www.m-p-r.com
Implant Resource Inc recalls MPR Slotted Mallets with potential head separation from handle and unexpected deformations. Affected units have model MPR-1120-1000 and lot numbers starting 200911-1-1. Contact 800.524.5194 for details.
MPRJul 21, 2021 - Stop using nowFood
Old Souls Farms LLC recalls Old Souls Farm Finstar 5 oz clamshells - 1oz 18 per case, 5oz 6 per case bulk bags - 1lb is 3 per case, 10lbs 1 per
Old Souls Farms recalls 5oz clamshells with Listeria monocytogenes detected in rainwater contact. Check lot codes on clamshells for affected products.
Old Souls FarmsJul 21, 2021 - Stop using nowConsumer product
Rite Aid Recalls Rechargeable Handheld Fans Due to Fire Hazard
Rite Aid recalls rechargeable handheld fans sold in blue, pink, and purple due to fire risk from lithium-ion battery overheating during charging. Consumers should stop using and get a refund.
Rite AidJul 21, 2021
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