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
34,894 found- Use cautionMeat & poultry
Rafedain Shish Kabob Restaurant, Inc. Recalls Chicken Patty Shish Kabob Products Due To Misbranding and Undeclared Allergens
USDA FSIS recalls 813 pounds of Rafedain chicken patty shish kabob products due to undeclared milk, wheat, and soy allergens. Consumers urged not to consume and dispose of items.
Rafedain Shish KabobDec 1, 2017 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device
Mindray recalls Gas Module 3 spirometers (part 115-030108-00) purchased between Feb 2008 and Oct 2015 due to regulatory changes requiring new safety approvals. This update ensures continued safe use in medical settings.
MindrayDec 1, 2017 - Use cautionMedical device
Ohmeda Medical recalls Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that
Ohmeda Medical recalls Rotating IV Poles with model 6600-0851-800 that may fall, risking injury to patients or staff. Affected units sold between specific lot codes.
Ohmeda MedicalDec 1, 2017 - Lower riskMedical device
Stryker Sustainability Solutions recalls 3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector. Intended for
Stry: 3040-VenaFlow Calf Garment (Aircast) was mislabeled as 3010-PL Aircast Pos-Lock Connector. This could cause confusion with a different product intended for DVT prevention. Affected units have UDI: 00885825016661.
StrykerDec 1, 2017 - Lower riskMedical device
Mako Surgical Corporation recalls RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Mako Surgical recalls RESTORIS MCK Tibial Baseplates with incorrect sizing labels that could lead to improper fit during knee replacement surgery. Affected items include specific sizes and lot numbers.
Mako SurgicalDec 1, 2017 - Use cautionMedical device
Elekta, Inc. recalls ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise
Elekta recalls Synergy, Synergy S, Synergy Platform, Precise, Infinity, Axesse, and Versa HD digital accelerators due to potential uncontrolled extension of iViewGT/XVI detector arms. Affected units may require repair or replacement.
Elek:taDec 1, 2017 - Stop using nowConsumer product
Camso Recalls Dirt to Snow Bike Conversion Kits Due to Crash and Impact Hazards
Camso recalls 2017 dirt to snow bike conversion kits due to brake pad pin loosening risks. Stop using immediately and get free repair.
CamsoDec 1, 2017 - Use cautionVehicle
HYUNDAI ELANTRA (2014) recall — Service Brakes, Hydraulic
Hyundai recalls 2013-2014 Elantra sedans for brake light switch issue causing lights to stay on and potential shift without braking, risking crashes. Fix available by February 2018.
HyundaiNov 30, 2017 - UnratedDrug
Intrathecal Compounding Specialist, LLC recalls All sterile drug preparations remaining within expiry prepared from Hydromorphone Base Solution dispensed between
Intrathecal Compounding Specialist recalls sterile drug preparations made from Hydromorphone Base Solution between Oct 2017 and Nov 2017 due to lack of sterility assurance. Affected items may cause infection if used.
Intrathecal Compounding SpecialistNov 30, 2017 - Stop using nowDrug
BYL Solutions Inc. recalls Bull Capsules, 1800 mg/grain, 30 count per tin, Hongkong Jiuyuejiu Biology Technology CO., LTD, BYL Solutions, Inc. dba
BYL Solutions recalls Bull Capsules (1800 mg/grain, 30 count) due to sildenafil contamination. Consumers should stop using these products immediately.
BYL SolutionsNov 30, 2017 - Lower riskFood
Raley's recalls Raley's All Butter Meyer Lemon Cookie; Case of Raw Dough (168 cookies) 28.87 lbs - UPC 10659728; 1 cookie (85 g); 6
Raley's recalls 168 cookies from 2017 that contain plastic material found in unbaked cookies at retail stores. Consumers should check for plastic pieces in the dough.
Raley'sNov 30, 2017 - Use cautionConsumer product
Natural Solutions for Life Recalls Synodrin Pain Relieving Cream Due to Failure to Meet Child Resistant Closure Requirement
Natural Solutions for Life recalls Synodrin Lidocaine Maximum Strength Pain Cream due to non-child-resistant packaging, risking poisoning for young children. Consumers should remove from reach and get free replacement cap.
Natural Solutions for LifeNov 30, 2017 - Stop using nowConsumer product
Kubota Recalls RTV-X Series Utility Vehicles Due to Injury Hazard (Recall Alert)
Kubota recalls RTV-X series utility vehicles with model numbers ending in 900, 1100, 1120D, or 1140 due to risk of seat belt stays breaking in crashes. Consumers should stop using and contact a dealer for free repair.
KubotaNov 30, 2017 - Use cautionConsumer product
Flos Recalls Pendant Light Fixtures Due to Impact Injury Hazard
Flos recalls Romeo Moon S2 and Romeo Louis II S2 pendant lamps due to glass diffuser detachment risk. Affected units may cause impact injuries if the plastic ring holding the glass is not securely attached.
FlosNov 30, 2017 - Use cautionVehicle
FORD EXPLORER (2016) recall — Seats
Ford recalls 2016 Explorer vehicles with loose power seat pivot bolts that may detach in crashes, increasing injury risk. Owners must have seats inspected by dealers for free.
FordNov 29, 2017 - Use cautionVehicle
FORD F-53 (2017) recall — Service Brakes, Hydraulic
Ford recalls 2017 F-53 trucks with potential brake fluid leaks causing longer stopping distances. Owners must have brake system inspected by dealers for missing valve plugs.
FordNov 29, 2017 - Use cautionVehicle
VOLKSWAGEN ATLAS (2018) recall — Fuel System, Gasoline
Volkswagen recalls 2018 Atlas vehicles with potential fuel leaks that could cause fire if near ignition sources. Owners must have fuel tank replaced free of charge by dealers.
VolkswagenNov 29, 2017 - Use cautionVehicle
TOYOTA 4RUNNER (2018) recall — Structure
Southeast Toyota recalls 2015-2018 Toyota 4Runners with Billet Grille Overlay that may detach while driving, increasing crash risk. Owners must have U-nuts replaced free by dealers starting January 26, 2018.
Southeast ToyotaNov 29, 2017 - Lower riskMedical device
Zimmer Dental Inc recalls Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSVTB10.
Zimmer Dental recalls Tapered Screw-Vent MTX dental implants (model TSVTB10) due to potential mislabeling from manufacturing mix-ups. Affected units may have incorrect thread diameters.
Zimmer DentalNov 29, 2017 - Lower riskMedical device
Smiths Medical ASD Inc. recalls BCI Advisor Vital Signs Monitor, Model 9200, Reorder numbers 920654235, 920654235, 920654335A, and 920674235A. (The
Smiths Medical recalls BCI Advisor 9200 Vital Signs Monitors with specific reorder numbers due to potential printing errors in tabular data, real-time continuous printouts, and automatic interrupt print features.
Smiths MedicalNov 29, 2017 - UnratedMedical device
Hologic, Inc. recalls Rapid for the TLiIQ(R) System, HOLOGIC(R), Catalog number: 01200
Hologic recalls Rapid cassettes (catalog 01200) due to unapproved material from a new supplier. This could pose risks if used without FDA approval. Affected users should check their model numbers.
HologicNov 29, 2017 - UnratedMedical device
Smith & Nephew, Inc. recalls smith&nephew, 2.4 MM, 6 HOLE, EVOS, FLEX PLATE, SST Plate, REF CATALOG NUMBER 72442360N, NON-STERILE, Rx only,
Smith & Nephew recalls EVOS 2.4mm Flex Plates with potential packaging templates that could cause injury during surgery. Affected items have catalog number 72442360N.
Smith & NephewNov 29, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Persona Partial Knee spacer block instruments; (1) 8mm block, Model Number: 42-5399-035-08; (2) 9mm block, Model
Zimmer Biomet recalls 8mm-14mm Persona partial knee spacer blocks that don't fit in alignment towers. These blocks are used in knee surgery to ensure proper bone resection. Affected models include specific sizes and lots.
Zimmer BiometNov 29, 2017 - Lower riskMedical device
Zimmer Biomet, Inc. recalls CPT 12/14 COCR SIZE 0 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Zimmer Biomet recalls hip implants with LDPE packaging that may leave residue on implants after removal. Affected units include specific lot numbers and sizes. Consumers should contact the company for details.
Zimmer BiometNov 29, 2017 - UnratedDrug
Blue Fusion Natural recalls BLUE PEARL capsules, 500mg, 1-count packets, Distributed by Blue Pearl Long Beach, CA UPC 8 4704600978 5
FDA recalls Blue Pearl 500mg capsules due to undeclared sildenafil, an unapproved drug with unknown safety. All units distributed by Blue Fusion Natural are affected.
Blue Fusion NaturalNov 29, 2017 - Use cautionDrug
Prinston Pharmaceutical Inc recalls Valsartan Tablets, USP, 160 mg, 90-count bottles, Rx Only, Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd,
Prinston recalls 21,987 bottles of Valsartan 160mg tablets due to failed specifications. Check your lot number and expiration date for details.
Prinston PharmaceuticalNov 29, 2017 - Lower riskFood
Donkey Salsa recalls SALSA HOT Net Wt. 15 oz (426 G)
Donkey Salsa recalls 15oz SALSA HOT products for possible plastic pieces. Consumers should check product codes 01-07 for affected items.
Donkey SalsaNov 29, 2017 - Stop using nowConsumer product
Toys“R”Us Recalls Clay Craft Kits Due to Risk of Mold Exposure; Sold at Babies“R”Us and Toys“R”Us
Toys R Us recalls Totally Me clay craft kits due to mold exposure risk. Stop using and return for refund if purchased Jan-Oct 2017.
Totally MeNov 29, 2017 - Stop using nowConsumer product
Libbey Glass Recalls Bourbon Glasses Due to Laceration Hazard
Libbey recalls 8oz Bourbon Taster Glasses with laser-etched logos that can break during normal use, causing lacerations. Return to retailer for refund.
Libb:eyNov 29, 2017 - Lower riskVehicle
ZERO S (2018) recall — Equipment
Zero is recalling certain 2018 motorcycles with misstated model years on emission labels, which may cause non-compliance with federal safety regulations. Owners should contact Zero for a corrected label.
ZeroNov 28, 2017
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