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 cautionVehicle
FORD F-550 (2018) recall — Exterior Lighting
Weis Fire & Safety is recalling one 2018 Ford F-550 emergency vehicle with Whelen brake lights that may illuminate without pressing the brake pedal, risking confusion for other drivers.
Weis Fire & SafetyMar 4, 2019 - Use cautionMedical device
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medtronic Pulmonary Vein Ablation Catheter(R) GOLD (PVAC GOLD) 990078 - Product Usage: The Pulmonary Vein Ablation
Medtronic recalls PVAC GOLD catheters (990078) produced in past 18 months without updated instructions to reduce phrenic nerve injury risk during heart procedures.
MedtronicMar 4, 2019 - Use cautionDrug
H J Harkins Company Inc dba Pharma Pac recalls Losartan Potassium 100 mg Tablets # 30 Losartan potassium tablets USP, 100 mg are white to off white, film coated, tear
Pharma Pac recalls 300 tablets of Losartan Potassium 100 mg due to NMBA impurity. Check your lot number LTO00EW and expiration date.
Pharma PacMar 4, 2019 - Use cautionDrug
Petra Hygienic Systems Int Ltd recalls ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan), 0.25%, 4 litres/1.1 US Gallon bottles, packaged in 4 x 4
Athleticare recalls Anti-Bacterial Hand Soap AC 550 because it contains triclosan, an ingredient no longer allowed in over-the-counter consumer antiseptic washes.
AthleticareMar 4, 2019 - Lower riskFood
Procesadora Aguas Claras LTDA. recalls Premium Sustainable Atlantic Salmon (Farm Raised); 22 lb. case - Master carton - corrugated cardboard box. Internal
Procesadora Aguas Claras LTDA. recalls 22-lb cases of farm-raised Atlantic salmon from Chile due to potential Listeria monocytogenes contamination. This product is for institutional use only.
Procesadora Aguas ClarasMar 4, 2019 - Lower riskMedical device
Viewray, Inc. recalls MRIdian Linac Radiation Therapy System Model 10000 and 20000
Viewray recalls specific MRIdian Linac models due to inadequate instructions for transferring radiation treatment plans between systems, potentially causing treatment errors. Affected units include Model 10000 and 20000 with listed serial numbers.
ViewrayMar 3, 2019 - Stop using nowMeat & poultry
Washington Beef, LLC Recalls Ground Beef Products due to Possible Foreign Matter Contamination
Washington Beef recalls ~30,260 lbs of ground beef chubs due to possible hard plastic and metal contamination. Do not consume.
Washington BeefMar 2, 2019 - Stop using nowFood
Surtidoras Bakery Inc recalls Vanilla Muffin, brand Surtidoras Bakery, net wt. 1.74 lbs., packaged in rigid plastic clam shell container. No UPC. The
Surtidoras Bakery Inc. recalls 1.74 lb vanilla muffins because milk is not listed in the Contains statement, posing a risk to those with dairy allergies.
Surtidoras BakeryMar 2, 2019 - Use cautionMedical device
Becton Dickinson & Company recalls BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog
Becton Dickinson recalls BD Nexiva Dual Port 20GA 1.00IN IV catheter systems due to potential blood exposure from leaks under high pressure during use.
Becton DickinsonMar 1, 2019 - Lower riskMedical device
Medical Action Industries Inc recalls Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)
Medical Action Industries recalls specific laparotomy sponges due to potential lack of sterility assurance. Affected models include Lap 18X18 XR with various model numbers and expiration dates. Consumers should check their product details to determine if they are affected.
Medical Action IndustriesMar 1, 2019 - Lower riskMedical device
Integra Limited recalls Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bioBLOCK Implant is
Integra recalls 10mm bioBLOCK resorbable subtalar implants with temperature indicator that may turn dark gray/black before shipment, indicating exposure to high temperatures.
IntegraMar 1, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to total hip implant Item
Zimmer Biomet recalls hip screws that may be mislabeled as 20mm when they are 30mm, risking surgical errors. Affected units include specific lot numbers. Contact for replacement.
Zimmer BiometMar 1, 2019 - UnratedMedical device
Thoratec Corp. recalls Thoratec HeartMate 3 Coring Tool, Sterile EO, Rx Only, REF 10005872, an optional accessory of Thoratec HeartMate 3 Left
Thoratec recalls HeartMate 3 Coring Tool (REF 10005872) due to small black plastic particles found in left ventricle during implant. Affected units have specific lot numbers.
ThoratecMar 1, 2019 - Lower riskDrug
Apotex Inc. recalls Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.03 mg, 28 Tablets Blister, 1 Unit (NDC 60505-4183-1) packaged
Apotex recalls 3 mg/0.03 mg contraceptive tablets due to missing or incorrect tablet placement in the blister pack. Consumers should check their packaging for NDC 60505-4183-1 or 60505-4183-3 and contact Apotex for details.
ApotexMar 1, 2019 - UnratedDrug
American Health Packaging recalls Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton (5 blister cards x 4 unit
American Health Packaging recalls Aspirin and Extended-release Dipyridamole Capsules due to potential unknown impurities in stability samples. Affected lots expire by March 2019.
American Health PackagingMar 1, 2019 - Lower riskDrug
AVKARE Inc. recalls Oxybutynin Chloride Extended-Release Tablets USP 10 mg, a) 100 tablets (NDC 42291-634-01) and b) 500 tablets (NDC
AVKARE recalls Oxybutynin Chloride Extended-Release Tablets USP 10 mg (100 and 500 tablets) due to failed dissolution specifications. These prescription-only tablets may not release medication properly.
AVKAREMar 1, 2019 - UnratedDrug
Legacy Pharmaceutical Packaging LLC recalls Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: The Kroger Co, Cincinnati, OH
Legacy Pharmaceutical Packaging LLC recalls Losartan Potassium Tablets (50mg) due to detected impurity NMBA. Affected lots: 180190, 180191 (exp 10/2020) and 181597 (exp 02/2021).
Legacy Pharmaceutical Packaging LLCMar 1, 2019 - Stop using nowDrug
Legacy Pharmaceutical Packaging LLC recalls Losartan Potassium Tablets, USP, 100 mg, 30 tablet bottles, Rx Only, Distributed by: Wal-Mart, Bentonville, AR 72716,
Legacy Pharmaceutical Packaging recalls Losartan Potassium 100mg tablets distributed by Wal-Mart due to the presence of impurity NMBA.
Legacy Pharmaceutical PackagingMar 1, 2019 - Stop using nowFood
Lamb Weston Inc recalls Lamb's Supreme Starz, item S0026, is formed star-shaped potato product that has been par-fried and frozen. Product is
Lamb Weston recalls frozen star-shaped potato patties due to foreign material contamination. Check your product for specific expiration dates and lot codes.
Lamb WestonMar 1, 2019 - Lower riskFood
Confections by Michael Recchiuti recalls Recchiuti Key Lime Apples; Net Wt: 4 oz. Crispy slices of Granny-Smith Apples in Semi-sweet chocolate. Ingredient: Dark
Recchiuti Confections recalls key lime apples with dark chocolate coating due to high milk protein levels found in one lot. Consumers should check for the specific product and follow safety steps.
Recchiuti ConfectionsMar 1, 2019 - Use cautionFood
Golden Gate Soy Products, Inc. recalls Garden Gate Tofu, Firm; Ingredients: Soybean, Filter water, Calcium Sulfate. Contains: soy Sold in 60 piece (bulk box)
Golden Gate Soy Products recalls Garden Gate Tofu Firm due to Listeria monocytogenes found on food contact surfaces. Products sold in 60-piece and 18-piece bulk boxes with specific expiration dates.
Golden Gate Soy ProductsMar 1, 2019 - Lower riskFood
Snow's Acquisition, LLC recalls Snow's PREMIUM ICE CREAM Mint Chip Mint Ice Cream with Dark Chocolate Chunks 1.5 QUART (1.42L) KEEP FROZEN, UPCE: 0
Snow's Premium Mint Chip Mint Ice: 1.5 quart ice cream with undeclared Yellow 5. Recall covers specific lot codes. Consumers should check labels for affected products.
Snow'sMar 1, 2019 - Lower riskFood
Cesar Iglesias, S.A. recalls El Rey Chocolitas 12.69oz (360gr) and 2.2lb (1 Kg)
Cesar Iglesias recalls El Rey Chocolitas 12.69oz and 2.2lb cereal due to undeclared soy lecithin. Consumers should check lot numbers and expiration dates for affected batches.
Cesar IglesiasMar 1, 2019 - Lower riskFood
Elite Spice Inc. recalls Basil Olive Oil Flavored Tortilla Seasoning Package Type: Box with liner, Units Per Case: 1, Weight Per Package: 50
Elite Spice recalls Basil Olive Oil Flavored Tortilla Seasoning (Lot 1-310242) due to undeclared milk allergen. Consumers should check packaging for lot number and contact Elite Spice for details.
Elite SpiceMar 1, 2019 - Use cautionVehicle
FREIGHTLINER M2 (2015) recall — Fuel System, Other
A-1 is recalling 2015 Freightliner M2 refuse trucks with CNG systems. If the valve knob is overtightened, the snap ring may fail, causing valve stem ejection and potential fire. Owners received notification letters in March 2019.
A-1Feb 28, 2019 - Use cautionVehicle
SUBARU CROSSTREK (2017) recall — Exterior Lighting
Subaru recalls 2017 Crosstrek models with brake lights that may not illuminate properly, increasing crash risk. Owners must have brake light switch replaced free by dealers.
SubaruFeb 28, 2019 - Stop using nowVehicle
MCLAREN 570 (2017) recall — Air Bags
McLaren is recalling 2017 570 vehicles with air bags that may explode due to propellant degradation from humidity and temperature. Owners must replace air bags free of charge.
McLarenFeb 28, 2019 - Use cautionVehicle
CHRYSLER PACIFICA (2018) recall — Suspension
Chrysler is recalling certain 2018 Pacifica vehicles due to a potential right front control arm separation that could increase crash risk. Owners must have their right front knuckle and lower control arm inspected by dealers for damage and replaced if needed at no cost.
ChryslerFeb 28, 2019 - Use cautionVehicle
RAM 1500 (2019) recall — Electrical System
Chrysler recalls certain 2019 Ram 1500 models with 48v auxiliary battery systems due to overheating risks that could cause cabin fires. Owners must have fasteners secured by dealers.
ChryslerFeb 28, 2019 - UnratedMedical device
Zimmer Biomet, Inc. recalls Biomet Small Diameter Cement Plug Inserter-Sterile, single-use accessory instrumentation to be used during surgical
Zimmer Biomet recalls sterile surgical cement plug inserters due to inadequate sterilization validation. Affected items were sold for surgical procedures. Consumers should contact the company for details.
Zimmer BiometFeb 28, 2019
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