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
34,896 found- Lower riskDrug
Apotex Inc. recalls Piperacillin and Tazobactam for Injection, USP 4.5 gram/vial* 10-count Single Use Vials per carton, Rx only, Mfg. by:
Apotex recalls 4.5g/vial Piperacillin-Tazobactam injections due to high impurities reducing drug potency. Patients should not use these products as they may not work effectively.
ApotexMay 8, 2018 - Use cautionFood
Sugarfina, LLC recalls Sugarfina Sugar Cookies Distributed by Sugarfina, Inc. small candy cube, large candy cube, and 1.0oz. taster packet UPC
Sugarfina recalls sugar cookies with undeclared egg allergen. Consumers should check UPC codes and stop using if allergic to egg.
SugarfinaMay 8, 2018 - Stop using nowConsumer product
Hauck Fun For Kids Recalls Go-Karts Due to Laceration and Collision Hazards
Hauck recalls Nerf Battle Racer go-karts (2016-2017) due to steering wheel detachment causing lacerations or collisions. Affected children should stop using and contact Hauck for a new steering wheel.
HauckMay 8, 2018 - Use cautionVehicle
JAYCO ALANTE (2019) recall — Visibility
Jayco is recalling 2019 Alante motorhomes with a wiper system that may lift at high speeds, reducing visibility and increasing crash risk. Owners must contact Jayco for free replacement.
JaycoMay 7, 2018 - Use cautionVehicle
JAYCO ALANTE (2019) recall — Equipment
Jayco is recalling 2018-2019 Alante motorhomes with incorrect cargo capacity labels that may cause vehicle overload and crash risk. Owners must contact Jayco for a corrected label.
JaycoMay 7, 2018 - Use cautionVehicle
ENTEGRA ANTHEM (2019) recall — Wheels
Entegra recalls 2018-2019 Anthem motorhomes for incorrect cargo capacity labeling, which may cause vehicle overload and crash risk. Owners must contact Entegra for a corrected label.
EntegraMay 7, 2018 - Use cautionVehicle
ENTEGRA VISION (2019) recall — Visibility
Entegra is recalling 2019 Vision motorhomes with a wiper system that may lift at high speeds, reducing visibility and increasing crash risk. Owners must have the wiper system replaced free by dealers.
EntegraMay 7, 2018 - Stop using nowMedical device
WRP Asia Pacific Sdn Bhd recalls AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112
Recalled AmerisourceBergen PF Latex SG surgical gloves (size 6.5) contain powder, which can cause latex allergies and severe reactions. Stop using immediately.
AmerisourceBergenMay 7, 2018 - Lower riskMedical device
Roche Diagnostics Hematology recalls cobas m 511 integrated hematology analyzer, Model Number 07261691190 Product Usage: The cobas m 511 integrated
Roche recalls cobas m 511 hematology analyzers that may give inaccurate results for patients with severe microcytic anemia, including iron deficiency and thalassemia. Affected units may need recalibration or software update.
Roche DiagnosticsMay 7, 2018 - Lower riskMedical device
Roche Diabetes Care, Inc. recalls Accu-Chek Performa Test Strip, Blood glucose monitoring system, Catalog no. 07299702001 Product Usage: The Accu-Chek
Roche recalls Accu-Chek Performa test strips that may cause inaccurate blood glucose readings, leading to incorrect health decisions. Affected lots include 476605. Consumers should check their test strip lot numbers.
RocheMay 7, 2018 - Lower riskMedical device
Ethicon, Inc. recalls PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031
Ethicon recalls PROLENE Suture Monobundle (BV1755 Taper Point 3/8C, D10031) due to packaging perforation risk. Perforated packaging may cause soft tissue injury or patient infection if sterility is breached.
EthiconMay 7, 2018 - Use cautionMedical device
Biosense Webster, Inc. recalls WaveCrest Left Atrial Appendage (LAA), Occlusion System (32 mm), Catalog Numbers WCR1523 and WCR2523.
Biosense Webster recalls WaveCrest Left Atrial Appendage (LAA) 32mm occlusion systems (catalog numbers WCR1523, WCR2523) due to risk of device failure during recapture attempts.
Biosense WebsterMay 7, 2018 - Lower riskDrug
Perrigo New York recalls Hydrocortisone Ointment, USP 2.5%, Net Wt. 20g, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed by
Perrigo recalls Hydrocortisone Ointment 2.5% (20g) due to failed stability specifications. This prescription-only product was manufactured in Bronx, NY with specific lot numbers and expiration dates. Consumers should check their product details and contact Perrigo for further instructions.
PerrigoMay 7, 2018 - Use cautionDrug
RIJ Pharmaceutical LLC recalls Geritrex Senna Syrup (sennosides 8.8mg), packaged in 8 FL OZ. (236 mL) bottle, Distributed by Geritrex, LLC 144
Geritrex recalls Senna Syrup due to CGMP deviations and out-of-spec microbial counts. Check lot numbers and expiration dates for affected bottles.
GeritrexMay 7, 2018 - Lower riskFood
Morgan Foods, Inc. recalls Great Value Gluten Free Tomato Condensed Soup, 10.5 oz, Number 1 Can, Two formats shipped: 8 cans per tray and 12 cans
Morgan Foods recalls Great Value Gluten Free Tomato Soup due to undeclared milk allergen. Consumers should check product codes and stop using if they have the affected items.
Morgan FoodsMay 7, 2018 - Use cautionVehicle
DUCATI SUPERSPORT (2018) recall — Fuel System, Gasoline
Ducati recalls 2017-2018 Supersport motorcycles due to fuel hoses near exhaust that may melt, causing leaks and fire risk. Owners must have hose routing checked by dealers.
DucatiMay 6, 2018 - Lower riskMedical device
Ortho-Clinical Diagnostics recalls VITROS Sodium Slides, Catalog # 837 9034
Ortho-Clinical Diagnostics recalls VITROS Sodium Slides (Catalog # 837 9034) due to potential for positively biased results. Affected units have specific UDI and expiry dates.
Ortho-Clinical DiagnosticsMay 5, 2018 - Stop using nowMeat & poultry
Eddy Packing Co., Inc. Recalls Smoked Sausage Products Due to Possible Foreign Matter Contamination
USDA FSIS recalls Eddy smoked sausage products from April 2018 due to possible hard plastic contamination. Consumers are urged not to consume these items and should discard or return them.
EddyMay 4, 2018 - Use cautionVehicle
CROSSROADS CRUISER (2018) recall — Service Brakes, Electric
Keystone recalls 2018 Crossroads Cruiser trailers with potential brake wire damage causing longer stopping distances and fire risk. Owners must contact customer service for free repairs.
KeystoneMay 4, 2018 - Use cautionVehicle
ACURA MDX (2018) recall — Seats
Honda recalls 2018 Acura MDX and Pilot/Ridgeline vehicles with potentially unsecured driver seats that could increase injury risk in crashes. Free seat frame replacements available.
HondaMay 4, 2018 - Use cautionVehicle
NEWMAR NEW AIRE (2019) recall — Tires
Newmar is recalling 2018-2019 New Aire motorhomes with specific wheels that may have valve stem damage causing tire overload and crash risk. Free replacement of stabilizers offered.
NewmarMay 4, 2018 - Lower riskMedical device
Smith & Nephew, Inc. recalls smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)
Smith & Nephew recalls Genesis II 13mm tibial punches with a 2mm size error that may cause improper fit during surgery. Affected units have specific reference number 71440408.
Smith & NephewMay 4, 2018 - Lower riskMedical device
Beckman Coulter Inc. recalls MicroScan Pos Combo Panel Type 43, Catalog number B1017-217for use in determining antimicrobial agent susceptibility
Beckman Coulter recalls MicroScan Pos Combo Panel Type 43 (B1017-217) due to incorrect Moxifloxacin dilution sequence, which may lead to inaccurate antimicrobial susceptibility testing results.
Beckman CoulterMay 4, 2018 - Lower riskMedical device
Synthes (USA) Products LLC recalls Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation.
Synthes recalls torque limiting handles with part number 03.231.013 due to potential rust from high-carbon ball bearings, which may affect fracture fixation systems.
SynthesMay 4, 2018 - Lower riskMedical device
Thermo Fisher recalls remel SUPERPACK CS/ 500 SEG/FLASK, REF R01626, Qty:50, plate label: REMEL MH W/OXACILLIN Product Usage: Recommended for
Thermo Fisher recalls 50 units of Remel SUPERPACK CS/500 SEG/FL: May fail performance testing for Staphylococcus aureus resistance. Consumers should check product labels for REF R01626 and lot 307200.
Thermo FisherMay 4, 2018 - Lower riskMedical device
Stryker GmbH recalls Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Stryker recalls Farabeuf Clamp for 3.5mm Screws PRO (Catalog # 705463) due to laser etching on the wrong side of the lever arm. This could cause incorrect mode detection during use.
StrykerMay 4, 2018 - Lower riskMedical device
Vascular Solutions, Inc. recalls Drainer(R) Centesis Catheters: (a) REF 8810, 5F x 9cm (b) REF 8811, 6F x 9cm (c) REF 8812, 5F x 15cm Product The
Vascular Solutions recalls Drainer centesis catheters (REF 8810, 8811, 8812) due to potential unsafe bacterial endotoxin levels in specific production lots. Affected lot numbers are listed for identification.
Vascular SolutionsMay 4, 2018 - Lower riskMedical device
Randox Laboratories recalls RX Imola (RX4900) For Professional Use for the quantitative in vitro determination of various clinical chemistry tests.
Randox recalls RX Imola (RX490:00) lab analyzers for professional use due to software issues that could delay test results. All units are affected.
RandoxMay 4, 2018 - Lower riskDrug
Noven Pharmaceuticals, Inc. recalls Minivelle (estradiol transdermal system) 0.1 mg/day, 1 System per pouch (NDC 68968-6610-1), packaged in 8 pouches per
Noven Pharmaceuticals recalls Minivelle estradiol patches due to adhesive issues that may cause patches to not stick well to skin. This is a drug product for hormone replacement therapy.
NovenMay 4, 2018 - Lower riskDrug
Milbar Laboratories, Inc. recalls MD Complete Clarifying Cleanser (Salicylic Acid 2.0%), 3 fl oz, (88.7mL), MD Professional LLC, Minneapolis, MN
Milbar recalls MD Complete Clarifying Cleanser (Salicylic Acid 2.0%) due to GMP deviations. This product may not meet quality standards, but no specific safety risks are described in the recall notice.
MilbarMay 4, 2018
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