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
35,025 found- UnratedDrug
Ummzy, LLC recalls Krazy Night capsule, packaged in a) 1-count per blister card and b) 10-count boxes, Manufactured by: SUM MARKETING LLC,
Ummzy recalls Krazy Night capsules (1-count blister cards and 10-count boxes) due to containing undeclared tadalafil/sildenafil/vardenafil without FDA approval. These products lack safety and efficacy data.
UmmzyMar 30, 2021 - UnratedDrug
Na Na Collection recalls Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW
Na Na Collection recalls Triple SupremeZen Gold 3500 capsules due to FDA finding unapproved drugs tadalafil and sildenafil. Consumers should check product details and contact the manufacturer.
Na Na CollectionMar 30, 2021 - Lower riskFood
USA LANKA INC recalls Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g,
USA LANKA INC recalls Motha Jelly Crystals due to undeclared and unapproved food dyes. Consumers should check product labels for batch numbers and expiration dates.
MothaMar 30, 2021 - Use cautionVehicle
FOREST RIVER BERKSHIRE (2021) recall — Exterior Lighting
Forest River recalls 2021 Berkshire Class A motorhomes with brake lights that don't reflect light well, risking crashes. Owners get free Reflex Reflectors.
Forest RiverMar 29, 2021 - Lower riskMedical device
Musculoskeletal Transplant Foundation, Inc. recalls AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous
Musculoskeletal Transplant Foundation recalls AFT Straight Tube (3/4 filled) due to potential surgery delay from improper filling. Affected units have specific lot numbers.
Musculoskeletal Transplant FoundationMar 29, 2021 - Lower riskMedical device
Philips North America Llc recalls Philips Xper Flex Cardio (FC2010, Procedure Room and FC2020, Bedside Monitor) devices - intended for use by
Philips recalls Xper Flex Cardio (FC2010/FC2020) monitors for possible display delays, data errors, and flat-line readings that could affect patient monitoring accuracy.
PhilipsMar 29, 2021 - Lower riskMedical device
Randox Laboratories Ltd. recalls Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator. Catalogue Number: CAL2351
Randox recalls Calibration Serum Level 3 (CAL 3) with batch 1162UE due to potential positive bias in bilirubin tests. Affected users should check their batch numbers and contact Randox for guidance.
RandoxMar 29, 2021 - Use cautionMedical device
Atos Medical AB recalls Provox Life Night HME, Catalogue Number 8262 - Product Usage: single use heat and moisture exchangers for patients
Atos Medical recalls Provox Life Night HME heat and moisture exchangers (catalog 8262) due to potential stoma blockage from incorrect insertion. Affected units: lot numbers 2012158 and 2012124.
Atos MedicalMar 29, 2021 - Lower riskMedical device
Greiner Bio-One North America, Inc. recalls VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,
Greiner Bio-One recalls VACUETTE blood collection tubes that may show insufficient draw volume, leading to inaccurate coagulation test results. Affected tubes have specific model numbers and expiration dates.
Greiner Bio-OneMar 29, 2021 - UnratedMedical device
Nobel Biocare Procera LLC recalls NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Product Usage: Implant Crown intended to be placed in the upper or lower jaw
Nobel Biocare recalls implant crowns not manufactured to specification. Affected units have material number 77364 and serial numbers starting with 173943753. Consumers should contact the manufacturer for details.
Nobel BiocareMar 29, 2021 - UnratedDrug
Spartan Chemical Co Inc recalls foamyiQ Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%), Net Contents: 42.27 oz/1250 ml per foam pump
Spartan Chemical recalls foamyiQ Lemon Blossom Hand Sanizer due to CGMP deviations. Check lot numbers and expiry dates for affected units.
foamyiQMar 29, 2021 - UnratedDrug
Teligent Pharma, Inc. recalls Lidocaine Ointment USP, 5%, NET WT 35.44 g (1 1/4 Oz) tube, Rx Only, Teligent Pharma Inc., Buena, New Jersey, 08310,
Teligent Pharma recalls 5% Lidocaine Ointment tubes due to failed stability tests. Product may not meet viscosity standards. No specific remedy stated in recall notice.
Teligent PharmaMar 29, 2021 - UnratedDrug
Nuri Trading LLC recalls Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC
Nuri Trading LLC recalls Shogun-X 7000 capsules due to undeclared tadalafil and sildenafil, unapproved drugs with unknown safety. All lots within expiry date.
Nuri Trading LLCMar 29, 2021 - Stop using nowFood
Richelieu Foods, Inc. recalls Tuscan Garden Ranch Dressing, packaged in 16 oz bottles, Dist. & Sold Exclusively by ALDI, Batavia, IL packaged in 12
ALDI sold Tuscan Garden Ranch Dressing with incorrect labels listing zesty Italian ingredients. This hides milk and egg, posing an allergy risk.
Tuscan GardenMar 29, 2021 - Use cautionVehicle
MERCEDES-BENZ AMG E53 (2021) recall — Seats
Mercedes-Benz recalls 2021 E53 AMG vehicles with passenger seats too close to airbag, increasing crash injury risk. Owners must have seat recalibrated by dealers.
Mercedes-BenzMar 26, 2021 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137
Siemens recalls Artis zee ceiling-interventional fluoroscopy systems with model 10094137 due to cable abrasion at the inner C-arm outlet, potentially requiring treatment cancellation or switch to alternative systems.
SiemensMar 26, 2021 - Lower riskMedical device
Radiometer Medical ApS recalls PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized, electrolyte-balanced, arterial blood sampler
Radiometer recalls PICO70 arterial blood samplers due to a remote risk of bacterial bloodstream infection, especially for immunosuppressed patients. The issue involves potential breaches in the sterile barrier system.
RadiometerMar 26, 2021 - Lower riskMedical device
ROi CPS LLC recalls Regard Dressing Change Tray
ROi CPS recalls Regard Dressing Change Trays with specific lot numbers due to potential package integrity issues from ChloraPrep applicators.
ROi CPSMar 26, 2021 - Lower riskMedical device
Nextremity Solutions recalls InCore Lapidus Disposable Kit 28mm Left, Part Number: IC-LAP-28L - Product Usage: Intended as a three-part construct
Nextremity Solutions recalls InCore Lapidus 28mm Left kit (part IC-LAP-28L) due to potential undersized drill bushing that may prevent surgical procedure completion.
Nextremity SolutionsMar 26, 2021 - Lower riskMedical device
Boston Scientific Corporation recalls The AMS 700 Inflatable Penile Prosthesis is a closed fluid-filled system containing saline. The system is made out of
Boston Scientific recalls AMS 700 penile prosthesis reservoirs mislabeled as 100 mL Conceal when they are 100 mL Spherical. This affects specific lot numbers and part numbers.
Boston ScientificMar 26, 2021 - Lower riskMedical device
Ortho-Clinical Diagnostics, INc. recalls VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the
Ortho-Clinical recalls VITROS Black Reference Slides (catalog J0231: 9252-0058-3361, 9252-0058-3362) due to incorrect labeling as White Reference Slides. Using these may cause delayed results for most tests.
Ortho-ClinicalMar 26, 2021 - Use cautionMedical device
Infusion Pump Repair recalls Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel repair part
Infusion Pump Repair Model 8100 pumps serviced with non-original bezel repair parts between Jan 2021 and March 2021 may crack, causing infusion interruptions. Affected units have specific serial numbers.
Infusion Pump RepairMar 26, 2021 - Lower riskMedical device
ConMed Corporation recalls KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line,
ConMed recalls certain KIT_INFINITY_BASE Custom Procedural Kits for possible lateral misalignment of tip guides, which may delay surgery or require alternative procedures.
ConMedMar 26, 2021 - Stop using nowDrug
Lupin Pharmaceuticals Inc. recalls Cefprozil for Oral Suspension USP, 250mg/5mL, packaged as a) 50 mL (when mixed) bottles (NDC 68180-402-01); b) 75 mL
Lupin Pharmaceuticals recalls specific lots of Cefprozil for Oral Suspension USP, 250mg/5mL, due to superpotent drug hazards. Check your NDC and lot numbers.
Lupin PharmaceuticalsMar 26, 2021 - UnratedDrug
Antoto-K recalls Thumbs Up 7 Red 70K, 10 count blister pack cartons, Distributed by Ummzy LLC., Made in USA, UPC 6 17135 89467 3.
Antoto-K recalls Thumbs Up 7 Red 70K 10-count blister packs due to FDA finding sildenafil and tadalafil without approved drug approval. All lots within expiry date.
Antoto-KMar 26, 2021 - Use cautionFood
Harris Teeter recalls HARRIS TEETER FRESH FOODS MARKET 3 Layer COOKIES & CREME CAKE NET WT 48 OZ (3 LB) 1.36kg packages PROUDLY DISTRIBUTED
Harris Teeter recalls 48oz cookies & creme cake packages containing undeclared hazelnuts. Consumers should avoid these products due to allergy risk.
Harris TeeterMar 26, 2021 - Lower riskFood
Sabra Dipping Company, LLC recalls Sabra Dipping Co, Classic Hummus ,10oz. PET cup, sealed with lid, 12 ct. Manufacturing Codes 300067. Expiration date
Sabra Dipping Company recalls 12-packs of Classic Hummus in 10oz PET cups with specific manufacturing codes due to potential Salmonella contamination. Consumers should check product details and follow official recall instructions.
SabraMar 26, 2021 - Use cautionVehicle
CHEVROLET COLORADO (2015) recall — Steering
GM recalls 2015 Chevrolet Colorado vehicles with potential power steering loss, increasing crash risk. Owners will receive free steering gear torque sensor cover assembly replacement.
ChevroletMar 25, 2021 - Use cautionVehicle
SPARTAN K2 (2022) recall — Steering
Shyft Group recalls certain 2021-2022 Spartan K2 RV Chassis vehicles due to potential steering output shaft disengagement causing loss of steering control.
Shyft GroupMar 25, 2021 - Use cautionVehicle
DUCATI MULTISTRADA (2021) recall — Engine
Ducati is recalling certain 2021 Multistrada V4 S motorcycles due to potential valve head failure that could increase crash risk. Owners must contact Ducati for free engine replacement.
DucatiMar 25, 2021
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