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- UnratedDrug
LUPIN SOMERSET recalls Gavilyte-N, PEG-3350, Sodium chloride, Sodium Bicarbonate and Potassium Chloride for Oral Solution, Rx only,
Lupin Somerset recalls Gavilyte-N packets because orange and cherry flavors incorrectly list 'natural lemon flavor' as an ingredient.
Lupin SomersetMar 19, 2019 - Lower riskFood
Merical, LLC recalls Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's
Walgreens recalls probiotic supplements because the product contains L. acidophilus La-5 instead of the labeled La-14 strain.
WalgreensMar 19, 2019 - Stop using nowConsumer product
Weatherbeeta USA Recalls Riding Saddles Due to Fall Hazard
Weatherbeeta USA recalls Collegiate riding saddles sold Aug 2016-Oct 2018. Short screws cause girth detachment, posing a fall hazard. Stop use and contact for free repair.
CollegiateMar 19, 2019 - Use cautionConsumer product
myStromer Recalls Electric Bicycles Due to Crash and Injury Hazards (Recall Alert)
Stromer recalls all ST5 electric bicycles due to potential stem breakage causing crashes and injuries. Affected models sold with black or gray aluminum frames have hydraulic disc brakes and integrated batteries.
StromerMar 19, 2019 - Use cautionVehicle
FORD TRANSIT (2018) recall — Seats
Quality Van recalls 2015-2018 Ford Transit vehicles with Freedman GO-ES Foldaway Seat cushions that may move during crashes, increasing injury risk. Owners must have seat inspected and repaired free by dealers.
Quality VanMar 18, 2019 - Use cautionVehicle
VOLVO VNL (2019) recall — Structure
Volvo recalls 2018-2020 VNL and VNX sleeper models with risk of window detachment causing crashes or injuries. Owners must have window hinge replaced free by dealers.
Volvo TrucksMar 18, 2019 - Use cautionVehicle
KIA SEDONA (2019) recall — Seat Belts
Kia recalls 2019 Sedona vehicles with improperly installed seat belt buckles that may prevent proper crash protection. Owners must have seat belts inspected and corrected free of charge.
KiaMar 18, 2019 - Use cautionVehicle
DUTCHMEN COLEMAN (2019) recall — Equipment
Keystone is recalling 2019 Dutchmen Aspen Trail trailers with Capital cooktops due to risk of excessive heat buildup causing burns. Owners must contact customer service for free replacement.
KeystoneMar 18, 2019 - Use cautionVehicle
MACK ANTHEM (AN) (2020) recall — Exterior Lighting
Mack recalls 2020 Anthem trucks with blocked rear reflectors that may reduce visibility, increasing crash risk. Owners must get free reflector installation by dealers.
MackMar 18, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Cios Alpha, Model Number 10308191 Mobile X-ray system - Product Usage: The Cios Alpha is a mobile X-Ray system designed
Siemens recalls specific Cios Alpha mobile X-ray systems (model 10308191) due to potential premature failure from continuous high-voltage use. Affected units may lose imaging capability.
SiemensMar 18, 2019 - Lower riskMedical device
Roche Diagnostics Corporation recalls Albumin BCP Product Usage: ALBP is an in vitro test used for the quantitative determination of albumin in human serum
Roche recalls Albumin BCP test kits due to calibration failures causing inaccurate albumin measurements. Affected lots may lead to incorrect test results for serum and plasma analysis.
RocheMar 18, 2019 - UnratedMedical device
Viewray, Inc. recalls MRIdian Linac Radiation Therapy System, Model 20000.
Viewray recalls its MRIdian Linac Radiation Therapy System Model 20000 due to potential dose calculation discrepancies between adaptive optimizations and AQA calculations. Affected units have specific serial numbers listed in the recall.
ViewrayMar 18, 2019 - UnratedMedical device
Advanced Bionics, LLC recalls HiResolution Bionic Ear System HiRes 90K Advantage CI HiFocus MS Electrode REF CI-1500-04. Cochlear Implant.
Advanced Bionics recalls HiRes 90K Advantage CI HiFocus MS Electrode cochlear implants due to missing bio-compatible materials in Japan's PMDA submission. Not distributed in the US.
Advanced BionicsMar 18, 2019 - Lower riskMedical device
Opgen Inc recalls CS011 GNR PNA FISH Control Slide, manufactured as a component of the CS011-10 GNR PNA FISH Control Slide kit . In-Vitro
Opgen recalls CS011 GNR PNA FISH Control Slide kits for possible diminished performance before expiration, leading to invalid test results for E. coli detection. Affected kits may need replacement to ensure accurate diagnostic results.
OpgenMar 18, 2019 - Lower riskMedical device
Ideal Implant Incorporated recalls IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes: 210cc, 240cc, 270cc, 300cc,
Ideal Implant recalls saline breast implants (210cc-675cc) due to silicone disrupting the posterior valve seal, causing deflation. Affected units have serial numbers 0100292-0102777.
Ideal ImplantMar 18, 2019 - Lower riskDrug
Ingenus Pharmaceuticals Llc recalls Diclofenac Sodium Topical Solution, 1.5% w/w, 5 FL. OZ. (150 mL) bottle, Rx Only, Manufactured for: Ingenus
Ingenus Pharmaceuticals recalls 1.5% diclofenac topical solution bottles that may leak, causing product contamination. Affected lots manufactured between 2019-2020 in Orlando, FL. Consumers should check lot numbers on bottles.
IngenusMar 18, 2019 - Stop using nowFood
Union Fish Company recalls Vega White Headless Shrimp, 21/15 and 26/30 count size. Frozen block in plastic bag, 6 x 4 lbs. per master carton.
Union Fish Company is recalling Vega White Headless Shrimp due to potential Salmonella contamination. Check your freezer for affected lots.
VegaMar 18, 2019 - Stop using nowFood
Almark Foods Inc recalls Nic's Peeled Pearls 20lb. Salad Grade Hard-Boiled Eggs NET WT. WHEN PACKED 20lbs Manufactured By: Almark Foods
Almark Foods recalls Nic's Peeled Pearls hard-boiled eggs due to positive Listeria monocytogenes test results. Check your lot numbers immediately.
Nic'sMar 18, 2019 - Use cautionMeat & poultry
Procesadora La Hacienda, Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
USDA FSIS recalls 4,940 pounds of corned beef products from Puerto Rico's Procesadora La Hacienda due to possible metal contamination. Products may contain metal pieces and should be thrown away or returned to purchase location.
Procesadora La HaciendaMar 15, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are
GE Healthcare recalls Panda Infant Radiant Warmers with model numbers M1112198-526438 and others due to risk of cracking if moved using bedside panels instead of handles. Check your unit's model number to see if it's affected.
GE HealthcareMar 15, 2019 - Use cautionMedical device
GE Healthcare, LLC recalls Innova IGS 6, Interventional Fluoroscopic X-Ray System used in generating fluoroscopic and rotational images of human
GE Healthcare recalls Innova IGS 6 X-Ray Systems that may lose imaging function when switching field of view from 30cm to 20cm or vice versa while releasing the footswitch pedal. Affected units have specific serial numbers.
GE HealthcareMar 15, 2019 - Lower riskMedical device
Response Biomedical Corp. recalls Randox Laboratories Ltd. Catalogue Number CQ5052, Lot Number 4244CK (relabeled as Response Biomedical Catalogue Number
Response Biomedical recalls Randox Cardiac Control (C2003-2) due to potential CK-MB level decreases in test results. Affected units have a 24-month shelf life and may cause inaccurate cardiac test results.
Response BiomedicalMar 15, 2019 - Lower riskMedical device
Cytocell Ltd. recalls Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent.
Cytocell recalls Aquarius CSF1R/RPS14 Probe Red reagent (model LPH540-A) with lot numbers 056996, 061156, 062616, 062808 due to a labeling error in the chromomap.
Cytoc:ellMar 15, 2019 - Lower riskMedical device
bioMerieux, Inc. recalls Biomerieux Vitek 2 Test kit VITEK 2 is an automated system consisting of instruments, software and reagent cards
Biomerieux recalls specific Vitek 2 test kits for potential ESBL bacteria misidentification risk in lab testing. Affected kits include AST-N254, AST-N330, and AST-N371 models with unique identifiers.
BiomerieuxMar 15, 2019 - Lower riskMedical device
Roche Diagnostics Corporation recalls cobas e 801 immunoassay analyzer
Roche recalls cobas e 801 immunoassay analyzers after complaints of signal drops during bottle changes, which could lead to incorrect medical decisions. Affected units may need repair or replacement.
RocheMar 15, 2019 - Use cautionMedical device
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER, 6F AL1.0, .070", REF SA6AL10. for cardiovascular use
Medtronic Vascular recalls SHERPA NX ACTIVE GUIDING CATHETER models with potential wire exposure. Learn what to do if you own this device for cardiovascular procedures.
Medtr:VascularMar 15, 2019 - UnratedDrug
Estee Lauder Inc recalls Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing
Estee Lauder recalls Repairwear Laser Focus Line Smoothing Cream SPF 15 due to ineffective cap seal. Consumers should check for light green folding carton with 50mL silver jar. No specific remedy stated in recall notice.
Estee La: LauderMar 15, 2019 - Use cautionDrug
Pfizer Inc. recalls 8.4% Sodium Bicarbonate Injection, USP 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL) 50 mL Single-dose fliptop vial, 25 vials
Pfizer recalls 25 vials of 8.4% Sodium Bicarbonate Injection with glass particulates. This injection may cause serious injury if used. Contact Pfizer for details.
PfizerMar 15, 2019 - UnratedDrug
Pfizer Inc. recalls Cleocin Phosphate, clindamycin injection, USP, 900 mg/ 6 mL (150 mg/mL), 6 mL vial, Rx only, Distributed by Pharmacia &
Pfizer recalls Cleocin phosphate injection due to impurities that could cause serious harm. Patients with prescription orders should check their medication details and contact Pfizer for guidance.
PfizerMar 15, 2019 - Use cautionFood
Nature's Touch Frozen Foods, LLC recalls O Organics Organic Whole Strawberries; NET WT. 48 oz. (3 lb.) 1.36 kg UPC: 079893402758 Distributed by: Lucerne Foods,
Nature's Touch Frozen Foods recalls organic strawberries with norovirus detected by FDA testing. Consumers should avoid eating these frozen berries due to potential illness risk.
Nature's TouchMar 15, 2019
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