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
35,006 found- Lower riskMedical device
Beckman Coulter Biomedical GmbH recalls DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, modular, automated
Beckman Coulter recalls DxA 5000 lab equipment due to unclear sample ID reuse instructions causing system failures. Affected units may need reconfiguration.
Beckman CoulterJun 17, 2020 - Stop using nowDrug
Preferred Pharmaceuticals, Inc. recalls Metformin HCl Extended Release Tablets, USP, 500 mg, Generic for Glucophage XR, Pkg Size 100, Mfg: Time-Cap, Labs Inc.,
Preferred Pharmaceuticals recalls 100-count Metformin HCl Extended Release Tablets due to detected N-Nitrosodimethylamine (NDMA) levels exceeding FDA safety limits. Consumers should stop using affected products immediately.
Preferred PharmaceuticalsJun 17, 2020 - Lower riskDrug
HF Acquisition Co. LLC recalls Famotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only After Dilution,
HF Acquisition Co recalls Famotidine injection vials due to temperature abuse complaints. Product received non-refrigerated, risking safety.
HF Acquisition CoJun 17, 2020 - Stop using nowFood
Brill Inc recalls Brill 30 lb. cases of 480 1.0 oz. chocolate chip with mini colored candy pieces frozen cookie dough, MDM # 10194626,
Brill Inc. recalls 30 lb cases of frozen cookie dough because they may contain undeclared walnuts, posing an allergy risk.
BrillJun 17, 2020 - Use cautionFood
Flagstone Foods LLC recalls NORTH STAR TRADING COMPANY SWEET & SALTY CARAMEL TRAIL MIX NET WT 14OZ (396g) MANUFACTURED FOR YOUR MILITARY EXCHANGES
Flagstone Foods recalls North Star Sweet & Salty Caramel Trail Mix due to undeclared cashews. Check your lot code and UPC for details.
North Star Trading CompanyJun 17, 2020 - Stop using nowConsumer product
Rexair Recalls to Repair Rainbow SRX Vacuums Due to Fire and Burn Hazards
Rainbow recalls SRX water-based vacuums with model RHCS19 Type 120 (serial 22003399-22077889) due to fire and burn risks from sparking circuit boards. Consumers must stop using and contact authorized distributors for free repairs.
RainbowJun 17, 2020 - Use cautionConsumer product
Republic Wireless Recalls Relay Charging Cables Due to Overheating and Burn Hazards
Republic Wireless recalls charging cables sold from May 2018 to May 2019 due to overheating and burn hazards. Affected cables lack the Relay logo on the charging head. Consumers should stop using and get free replacements.
Republic WirelessJun 17, 2020 - Stop using nowConsumer product
HON Recalls Office Chairs Due to Fall Hazard
HON recalls office chairs with model numbers HGTMM, HGV1MM, and M-SEMO201, M-SEMX101 made between Feb 2019 and Feb 2020 due to risk of back breaking and falls.
HONJun 17, 2020 - Use cautionConsumer product
Edwards Recalls Mechanical Heat Detectors Due to Failure to Alert to Fire
Edwards recalls mechanical heat detectors that may fail to alert to fires, posing a risk of undetected fire in residential and commercial settings. Affected units include specific models sold through retailers like Grainger and Interlogix.
EdwardsJun 17, 2020 - Use cautionVehicle
COACHMEN PRISM (2020) recall — Equipment
Forest River recalls 2020 Coachmen Prism RVs with incorrect Auto-P function in operator's manual, risking rollaway. Owners get corrected manual via email or dealer.
Forest RiverJun 16, 2020 - Lower riskMedical device
Synthes Produktions GmbH recalls MatrixMIDFACE Screws - Product Usage: The intended use for this device is in fixation of cranial bones and facial
Synthes recalls MatrixMID: 1.8mm emergency screws with a 3mm instead of 12mm clip marking. This mismatch could lead to improper bone fixation during surgery. Affected units include Lot #41P2340.
SynthesJun 16, 2020 - Use cautionMedical device
CME America, LLC recalls BodyGuard Microset, REF: A120-161XPS
CME America recalls BodyGuard Microset (REF: A12:161XPS) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry date.
CME AmericaJun 16, 2020 - Lower riskDrug
Glaxosmithkline Consumer Healthcare Holdings recalls Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ
Glaxosmithkline recalls Childrens Dimetapp Cold & Cough bottles for ages 6+ due to missing graduations on dosing cups, which could lead to incorrect dosing for younger children.
Glaxosmithkline Consumer HealthcareJun 16, 2020 - Lower riskDrug
SCA Pharmaceuticals recalls Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx Only, SCA Pharmaceuticals 755 Rainbow
SCA Pharmaceuticals recalls Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bags due to subpotent drug results at 30-day stability. This affects Rx-only products with specific lot numbers.
SCA PharmaceuticalsJun 16, 2020 - Lower riskFood
He Butt recalls Hill Country Fare Citrus Punch Drink 1 GAL CONT. NET. 3.78L Contains 0% Juice UPC 4122081863
He Butt recalls Hill Country Fare Citrus Punch Drink (1 gal, UPC 4122081863) due to potential undeclared milk. Consumers should check if they have this product and contact He Butt for details.
He ButtJun 16, 2020 - Use cautionVehicle
BMW X3 (2020) recall — Steering
BMW is recalling 2020 X3 models with a potential steering tie rod fracture risk in high heat or rough conditions, which could cause a crash. Owners must contact BMW or Toyota for free replacement.
BMWJun 15, 2020 - Lower riskMedical device
Access Scientific LLC recalls POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell Catheter made of ChronoFlex C with BioGUARD
Access Scientific recalls POWERWAND XL 4Fr 10cm Maximum Barrier Kit due to mislabeled catheter length, which could cause treatment delays or user dissatisfaction. No immediate action needed.
Access ScientificJun 15, 2020 - Lower riskMedical device
Luminex Corporation recalls Verigene Processor SP with assay Luminex, VERIGENE Gram-Negative Blood Culture Nucleic Acid Test, BC-GN, IVD - Product
Luminex recalls Verigene Processor SP devices with specific serial numbers that may produce false negative results for Gram-Negative Blood Culture tests, potentially leading to missed infections. Affected units include those with serial numbers listed in the recall.
LuminexJun 15, 2020 - Stop using nowMeat & poultry
Lakeside Refrigerated Services Recalls Beef Products due to Possible E.coli O157:H7 Contamination
USDA recalls 42,922 lbs of ground beef products from Lakeside Refrigerated Services due to possible E. coli O157:H7 contamination. Consumers are urged not to consume these products and should dispose of or return them.
Lakeside Refrigerated ServicesJun 13, 2020 - Stop using nowDrug
Yusef Manufacturing Laboratories, LLC recalls Tropical Lip Moisturizer, SPF 30, UVA/UVB Lip Protection, Active Ingredients: Oxybenzone 5%, Octisalate 5%, Octinoxate
Yusef recalls Tropical Lip Moisturizer SPF 30 due to potential superpotent drug levels in some batches. This may cause serious health effects if used as intended.
YusefJun 13, 2020 - Use cautionMedical device
Medtronic Xomed, Inc. recalls Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,
Medtronic Xomed recalls specific IPC software versions due to potential M5 Microdebrider rotating at higher speed than set during surgical procedures. Affected units include model 1898072 with listed lot numbers.
Medtronic XomedJun 12, 2020 - Lower riskDrug
Aurobindo Pharma USA Inc. recalls Clozapine Tablets USP tablet, 100mg, 500-count bottle, Rx only, Distributed by: Aurobindo Pharma USA, Inc. 279
Aurobindo Pharma USA recalls 100mg Clozapine tablets (500-count) after consumer complaints of 50mg tablets being present in some bottles.
Aurobindo PharmaJun 12, 2020 - UnratedDrug
The Harvard Drug Group recalls Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 100 Tablets (10 x 10) unit dose cartons, Rx only,
The Harvard Drug Group recalls Metformin Hydrochloride Extended-Release Tablets (500mg) due to potential presence of NDMA impurity above safe levels. This recall affects specific lot numbers and distribution channels.
The Harvard Drug GroupJun 12, 2020 - Lower riskDrug
Beaming White Llc recalls Koala Hand Sanitizer, Soothing Eucalyptus, 16 FL OZ., Antibacterial, (Ethyl Alcohol 68%), Manufactured by Beaming White
Beaming White recalls Koala Hand Sanitizer due to ethanol content below label claims and undeclared isopropyl alcohol. Consumers should check product details and contact for remedy.
Beaming WhiteJun 12, 2020 - Lower riskFood
NOW Health Group Inc. recalls NOW Real Food Raw Macadamia Nuts Unsalted 8 oz retail bag UPC 733739071194 Item number 7119
NOW Health Group recalls unsalted macadamia nuts due to Salmonella contamination. Consumers should avoid using these products to prevent foodborne illness.
NOW Health GroupJun 12, 2020 - Use cautionVehicle
FOREST RIVER ROCKPORT (2019) recall — Electrical System
Forest River recalls 2019-2020 Rockport work trucks with potentially inadequately welded battery boxes that could detach, increasing crash risk. Owners should contact customer service for free inspection or repair.
Forest RiverJun 11, 2020 - Use cautionVehicle
AUTOCAR XPEDITOR (2021) recall — Suspension
Autocar is recalling 2020-2021 Xpeditor vehicles with potentially loose suspension bolts that could cause crashes or injuries. Owners must have bolts inspected and tightened by dealers.
AutocarJun 11, 2020 - Use cautionVehicle
AUTOCAR XPEDITOR (2021) recall — Engine
Autocar is recalling 2020-2021 Xpeditor vehicles with X12N engines due to a short ground cable that may fail, causing engine stalling and crash risk. Owners must contact Autocar for free replacement.
AutocarJun 11, 2020 - Lower riskMedical device
Smiths Medical ASD Inc. recalls PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.
Smiths Medical recalls PORT-A-CATH II Power PAC Low Profile System with 8Fr catheter instead of 6Fr. Affected units may cause complications during procedures.
Smiths MedicalJun 11, 2020 - Lower riskDrug
Hikma Pharmaceuticals USA Inc. recalls Irinotecan HCL Injection, USP, 100mg/5mL, 5 mL vials, Rx only, Manufactured by: Thymoorgan Pharmazie GmbH, Shiffgraben
Hikma Pharmaceuticals recalls Irinotecan HCL injection vials due to crimp defect causing flip-cap removal issues. Affected lots expire 08/2021 or 09/2021.
Hikma PharmaceuticalsJun 11, 2020
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