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
34,959 found- Use cautionFood
Hikari Miso International, Inc. recalls Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
Hikari recalls Enjuku Koji Miso Mutenka due to missing English labeling that fails to declare soy, a major allergen.
HikariFeb 1, 2019 - Stop using nowFood
Whole Foods Market recalls Whole Foods Hipster Chipster Cookies; 9 oz. container with 6 cookies; UPC 0247449 006990 Sold at Whole Foods, Yulupa
Whole Foods Market recalls Hipster Chipster Cookies due to undeclared walnuts causing anaphylactic reactions. Check UPC 0247449 006990 for affected items sold at Whole Foods locations.
Whole Foods MarketFeb 1, 2019 - Use cautionPet food
Hill's Science Diet – Canned Dog Food: Potentially Elevated Levels of Vitamin D
Hill's voluntarily recalls select canned dog foods due to potentially elevated vitamin D levels that may cause vomiting, loss of appetite, and kidney issues in dogs. Affected products include specific sizes and lot codes.
Hill'sJan 31, 2019 - Stop using nowVehicle
MERCEDES-BENZ SPRINTER (VS30) (2019) recall — Steering
Mercedes-Benz Sprinter 2019 models with steering shaft disconnect risk sudden loss of control. Owners must stop driving immediately and have steering bolts inspected by dealers.
Mercedes-BenzJan 31, 2019 - Lower riskMedical device
Microbiologics Inc recalls Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
Microbiologics recalls Cepheid Respiratory Control Panel (Catalog #8199) due to reduced expiration date from 24 months to 13 months for in vitro diagnostic use.
MicrobiologicsJan 31, 2019 - Lower riskMedical device
RHONDIUM LIMITED recalls Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is
Rhondium recalls OVC3 One Visit Crowns with incorrect expiration dates. Affected units may have safety risks due to mislabeling.
RhondiumJan 31, 2019 - Use cautionMedical device
Medline Industries Inc recalls Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two
Medline recalls two models of 3000cc suction canisters (OR530, OR530H) due to potential lid fragmentation during use. Affected units sold with specific lot numbers from 20180913-1 to 20180929-1.
MedlineJan 31, 2019 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By: Dr. Reddy's Laboratories
Dr. Reddy's recalls 250mg Divalproex Sodium Extended-release Tablets due to failed dissolution testing. This may affect medication effectiveness. Contact for return instructions.
Dr. Reddy'sJan 31, 2019 - Use cautionVehicle
BMW X1 (2019) recall — Exterior Lighting
BMW is recalling certain 2018-2019 X1 models due to taillight attachment brackets that may crack, causing lights to loosen or detach and increasing crash risk. Owners should contact BMW for free repairs.
BMWJan 30, 2019 - Lower riskMedical device
U&I CORP. recalls Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 -
U&I CORP. recalls Velofix SA cervical cages with specific reference numbers due to potential screw pullout or instability. Affected models may not engage bone properly as intended by physicians.
U&I CORP.Jan 30, 2019 - Lower riskMedical device
Matrix Surgical Holdings, LLC recalls OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: OmniPore Surgical Implants in block, sheet, and
Matrix Surgical Holdings recalls OmniPore Surgical Implants Petite Paranasal - Left for mislabeling. This affects specific lot numbers used in craniofacial reconstruction. Consumers should contact the manufacturer for details.
Matrix Surgical HoldingsJan 30, 2019 - Lower riskDrug
Valeant Pharmaceuticals North America LLC recalls Cardizem CD (diltiazem HCl) capsules, 120 mg, packaged in a) 30-count bottles (NDC 0187-0795-30); and b) 90-count
Valeant recalls Cardizem CD 120mg capsules (NDC 0187-0795-30 and 0187-0795-42) due to failed dissolution testing. These capsules may not release medication properly, potentially affecting treatment effectiveness.
ValeantJan 30, 2019 - Lower riskFood
1908 Brands recalls Bundle Organics Bar Salty Nuts and Seeds, 1.9 Oz snack bar, Ambient storage
1908 Brands recalls Bundle Organics Salty Nuts and Seeds snack bars due to mold contamination. Affected lots include 2888, 2912, 2915, 2942, 2943. Consumers should check packaging for lot numbers and discard if mold is present.
1908 BrandsJan 30, 2019 - Stop using nowFood
Dunkin Brands Inc recalls DUNKIN' DONUTS MULTIGRAIN BAGEL DOUGH PRODUCT APPROVED BY: DUNKIN'DONUTS Unit wt: 4.5oz Count: 104 units Net Wt: 29 lb
Dunkin' Donuts recalls multigrain bagel dough products due to potential foreign material contamination. Check lot numbers and distribution details.
Dunkin' DonutsJan 30, 2019 - Stop using nowConsumer product
Hot Mom Recalls Bed Rails Due to Violation of Federal Standard for Portable Bed Rails: Sold Exclusively on Amazon.com (Recall Alert)
Hot Mom recalls bed rails with model number Boom09 sold on Amazon due to entrapment and suffocation hazards for young children. Consumers must stop using and return for refund.
Hot MomJan 30, 2019 - Stop using nowMeat & poultry
Tyson Foods, Inc. Recalls Chicken Nugget Products due to Possible Foreign Matter Contamination
Tyson Foods recalls 36,420 pounds of chicken nuggets from Nov. 2018 production due to possible rubber contamination. Consumers urged not to eat or dispose of recalled items.
TysonJan 29, 2019 - Use cautionVehicle
ACURA TLX (2019) recall — Fuel System, Other
Honda recalls 2019 Acura TLX models with potential fuel pump issues causing engine stalling and crash risk. Free software update or fuel pump replacement available.
HondaJan 29, 2019 - Lower riskMedical device
COLLINS AEROSPACE recalls TASE 400 Imaging systems
Collins Aerospace recalls TASE 400 Imaging systems due to a miscalculated Nominal Ocular Hazard Distance (NOHD) in Class lllb alignment lasers. This could pose a risk of eye injury during normal use. Affected units may need to be returned or repaired.
Collins AerospaceJan 29, 2019 - Lower riskDrug
US Compounding Inc recalls Ephedrine Sulfate, 50 mg/10 mL, 10 mL Single Use Syringe, Rx only, US Compounding Pharmacy 1270 Don's Lane Conway, AR
US Compounding Inc recalls 50 mg/10 mL Ephedrine Sulfate syringes due to lack of sterility assurance. This may cause infections if used improperly. Contact for details.
US Compounding IncJan 29, 2019 - UnratedFood
Prolacta Bioscience recalls Prolact CR; Human Milk Caloric Fortifier (Human, Pasteurized); Product Code: 94000-10 4 - 10 mL (0.3 fl. oz) Bottles,
Prolacta Bioscience recalls human milk caloric fortifier bottles due to unconfirmed shipment issues. Affected products were shipped under quarantine pending investigation. Consumers should check product codes and contact the company for details.
Prolacta BioscienceJan 29, 2019 - Stop using nowMeat & poultry
Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens
Perdue Foods recalls ~16,011 lbs of refrigerated Fun Shapes Chicken Breast Nuggets due to undeclared milk. Do not consume; return or discard.
PerdueJan 28, 2019 - Use cautionVehicle
GILLIG LOW FLOOR (2016) recall — Steering
Gillig is recalling certain 2016-2018 Low Floor buses due to potential steering instability from improperly tightened ball studs. Owners should contact Gillig for free inspection and correction.
GilligJan 28, 2019 - Use cautionVehicle
AUDI S8 (2016) recall — Fuel System, Gasoline
Audi is recalling 2016 S8 vehicles with a potential fuel leak that could cause fire if near ignition sources. Owners must have a fuel pressure damper installed by dealers.
AudiJan 28, 2019 - Use cautionVehicle
KEYSTONE MONTANA (2019) recall — Structure
Keystone is recalling 2019 Montana RVs with model 3855BR/3854BR due to a risk of tire failure from adjustment bolt contact. Free replacement of parts available.
KeystoneJan 28, 2019 - Use cautionMedical device
Applied Medical Resources Corp recalls Kii Fios First Entry, 5 X 75 mm, RX only, REF CFF05 Qty: 6, Sterile R, Lot: 1330981, Exp: July 15, 2021, Applied
Applied Medical Resources recalls Kii Fios First Entry surgical devices (Lot 1330981, exp July 2021) due to potential non-sterility, risking patient infection. Affected users should contact the company for details.
Applied Medical ResourcesJan 28, 2019 - Lower riskMedical device
LivaNova USA Inc. recalls LivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The
LivaNova recalls S5 systems with incorrect manufacturing date labels. Some devices show dates in yy-mm-dd format instead of yyyy-mm-dd. Affected units may have labeling errors that could cause confusion during use.
LivaNovaJan 28, 2019 - Lower riskMedical device
Spacelabs Healthcare, Inc. recalls Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.
Spacelabs Healthcare recalls Model 92810 Smart Disclosure System software versions 5.00-5.03 that may print patient waveforms from another patient's records.
Spacel:labsJan 28, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls ACUSON NX2 Elite Diagnostic Ultrasound System, Model # 11284500, RX Only, Siemens Medical Solutions, containing
Siemens recalls ACUSON NX2 Elite ultrasound systems with specific software versions due to potential transducer power exceeding safety limits. Affected units may have risks during use; contact for remedy.
SiemensJan 28, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Bimatoprost Ophthalmic Solution 0.03%, packaged in a) 5 mL (NDC 68180-429-02) and b) 7.5 mL (NDC 68180-429-03) bottles,
Lupin Pharmaceuticals recalls 0.03% Bimatoprost Ophthalmic Solution in 5mL and 7.5mL bottles due to impurities. This may cause eye irritation or other issues. Stop using and contact for replacement.
Lupin PharmaceuticalsJan 28, 2019 - Use cautionMeat & poultry
Harvest Food Group, Inc. Recalls Poultry Products Due to Misbranding and Undeclared Allergen
USDA FSIS recalls 47,332 pounds of chicken fried rice products for containing undeclared milk, a known allergen. Consumers urged to discard or return products.
Harvest Food GroupJan 25, 2019
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