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
34,956 found- Lower riskMedical device
Becton, Dickinson and Company, BD Biosciences recalls BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number 662878 BD FACSLyric is a high-performance
BD Biosciences recalls BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1 due to Windows 10 OS not being approved for clinical use. Affected units have specific serial numbers and catalog numbers.
BD BiosciencesJan 2, 2019 - Stop using nowMedical device
Leica Microsystems, Inc. recalls Leica M220 F12 surgical microscope The Leica M220 F12 surgical microscope is an optical instrument for improving the
Leica Microsystems recalls M220 F12 surgical microscopes due to risk of unintended drops into surgical field. Affected units have specific serial numbers. Contact Leica for details.
LeicaJan 2, 2019 - Stop using nowDrug
Baxter Healthcare Corporation recalls Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5% Dextrose, 2000 mL UltraBag container bag, Rx
Baxter recalls Dianeal Low Calcium peritoneal dialysis solution with leaks in tubing. Affected units have specific product codes and lot numbers. Stop using immediately to prevent infection.
Baxter HealthcareJan 2, 2019 - Lower riskDrug
PharMEDium Services, LLC. recalls 0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate) a.) 1 mL in 3 mL BD Syringe, 10 per carton, b.) 0.9%
PharMEDium Services recalls 0.9% buffered lidocaine HCl syringes due to subpotent risk. Affected products include specific syringe models sold in cartons with serial numbers starting 183320004S.
PharMEDiumJan 2, 2019 - Stop using nowDrug
Hiers Enterprises, LLC dba Northwest Compounding Pharmacy recalls Methocarbamol liquid 100mg/ml, RX, glass vial
Hiers Enterprises recalls Methocarbamol liquid 100mg/ml from Oregon due to lack of sterility assurance. Check lot numbers and expiration dates.
Northwest Compounding PharmacyJan 2, 2019 - Lower riskDrug
Heritage Pharmaceuticals, Inc. recalls Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials, Rx only, Mfd by: Emcure Pharmaceuticals Ltd.,
Heritage Pharmaceuticals recalls Cidofovir injection vials (NDC 23155-0216-31) because dried powder on the outside of bottles may indicate lack of sterility. This is a prescription-only medication.
Heritage PharmaceuticalsJan 2, 2019 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP, 125mg/5mL, packaged in a) 60mL (NDC 68180-722-20), b)100mL (NDC 68180-722-10), Rx
Lupin Pharmaceuticals recalls Cefdinir oral suspension (125mg/5mL) due to thickened suspension after reconstitution. Affected lots from January to May 2019. Consumers should check NDC codes and lot numbers for affected products.
Lupin PharmaceuticalsJan 2, 2019 - Use cautionVehicle
SUBARU BRZ (2018) recall — Visibility
Subaru recalls 2018 BRZ vehicles with backup camera that fails to display rearview image while reversing, risking crashes. Owners must contact Subaru for free software update.
SubaruDec 31, 2018 - UnratedMedical device
KaVo Dental Technologies LLC recalls cone-beam CT system
KaVo Dental recalls cone-beam CT systems with firmware versions 2.1.0 and 2.1.1 due to a defect that may cause improper imaging. Affected units should be checked for the specific firmware versions.
KaVo DentalDec 31, 2018 - Use cautionDrug
Aurobindo Pharma USA Inc. recalls Valsartan Tablets USP 40 mg, 30 count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., Dayton, NJ --- NDC
Aurobindo Pharma recalls specific lots of Valsartan Tablets USP 40 mg due to trace amounts of the impurity NDEA found in the manufacturing process.
Aurobindo PharmaDec 31, 2018 - Stop using nowDrug
Aurobindo Pharma USA Inc. recalls Valsartan tablets USP 320 mg, 90-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc., Dayton, NJ
Aurobindo Pharma recalls 320mg Valsartan tablets with NDEA impurity above safe levels. FDA confirmed impurity in API used for manufacturing. Stop using immediately if you have these specific lots.
Aurobindo PharmaDec 31, 2018 - Stop using nowFood
Willamette Valley Pie Company, LLC. recalls IQF Red Raspberries, packed in flexible poly bags, net wt. 2 lbs. per bag. There are six bags packed per case. UPC is 0
Willamette Valley Pie Company recalls IQF Red Raspberries due to potential Norovirus contamination. Check lot codes and UPCs immediately.
Willamette Valley Pie CompanyDec 31, 2018 - Stop using nowMeat & poultry
R. L. Zeigler Co., Inc. Recalls Chicken and Pork Red Hot Sausage Products due to Possible Foreign Matter Contamination
USDA FSIS recalls 11,664 pounds of chicken and pork red hot sausages from 2018 due to possible metal contamination. Consumers urged not to eat and dispose of products.
R. L. Zeigler Co.Dec 30, 2018 - Use cautionVehicle
HYUNDAI SANTA FE SPORT (2014) recall — Engine
Hyundai is recalling 2014 Santa Fe Sport vehicles with a potential fuel leak risk that could cause fire if an ignition source is present. Owners must have the fuel pipe inspected and replaced free of charge.
HyundaiDec 28, 2018 - Use cautionMedical device
Fetzer Medical GmbH & Co. KG recalls 12002 / Boss Instruments Simpson OB Forceps, short model, 13" (33cm), Item No./Product Code 46-5040 Fetzer Medical
Fetzer Medical recalls 13" OB forceps (model 46-5040) due to doctors being unable to separate the instruments during childbirth. Affected units sold with lot number 13300956.
Fetzer MedicalDec 28, 2018 - Lower riskMedical device
GE Healthcare, LLC recalls GE HEALTHCARE LOGIQ P6 Premium TruScan(TM) Imagining Technology: (a) Model BT09 (b) Model BT07 Product Usage: The
GE Healthcare recalls Logiq P6 Premium TruScan ultrasound systems with models BT07 and BT09 due to increased probe-head temperature during specific scans and with certain probes. Affected units have serial numbers listed in the recall notice.
GE HealthcareDec 28, 2018 - Stop using nowFood
Salmon River Foods Inc recalls The Forest Wild Collection Dark Chocolate bar, CB15052, net wt. 1.25 oz per bar. Product is packaged in a card board
Salmon River Foods recalls The Forest Wild Collection Dark Chocolate bars due to undeclared milk. Check your UPC and lot codes for details.
The Forest Wild CollectionDec 28, 2018 - Use cautionVehicle
FOREST RIVER SALEM (2019) recall — Electrical System
Forest River recalls 2019 Salem trailers due to power cord melting near water heater exhaust, risking fire. Owners must secure cord away from exhaust.
Forest RiverDec 27, 2018 - Lower riskMedical device
Cardinal Health 200, LLC recalls Curity All Purpose Sponges, Non-woven, 4 Ply, 4" x 4" (10.2 cm x 10.2 cm) Product Code: 8044 - Product Usage: Ideal for
Cardinal Health recalls non-sterilized Curity All Purpose Sponges (Product Code 8044) due to improper sterilization. These sponges may pose infection risks if used for medical purposes.
Cardinal HealthDec 27, 2018 - Use cautionVehicle
SPARTAN METROSTAR (2017) recall — Service Brakes, Air
Spartan recalls 2017 Metrostar vehicles with brake release delays that could increase crash risk. Owners must contact Spartan for free brake system repairs by February 22, 2019.
SpartanDec 26, 2018 - Use cautionMedical device
Steris Corporation recalls ATLAS Loading Car
Steris recalls ATLAS Loading Cars with specific serial numbers due to potential sliding or falling when empty, which could cause injury. Affected units include serial numbers listed in the recall notice.
SterisDec 26, 2018 - Use cautionMedical device
WEST PHARMA. SERVICES IL, LTD recalls Vial2BAG DC 13mm, REF 6070111, Single use only, Rx Only
West Pharma Services recalls Vial2BAG DC 13mm (REF 6070111) due to potential inadequate mixing of oxytocin with IV solution, which could cause concentrated drug pooling and bolus injections in pregnant women.
West Pharma ServicesDec 26, 2018 - Lower riskMedical device
Luminex Corporation recalls Vergene Amplification Tray - 700uL, BC-GP REF 20-011-018 The Verigene(R) Gram-Positive Blood Culture Nucleic Acid Test
Luminex recalls Vergene Amplification Tray (700uL, BC-GP REF 20-011-018) due to labeling error on Verigene Gram-Positive Blood Culture Nucleic Acid Test kits. Affected units have specific UDI and lot numbers.
LuminexDec 26, 2018 - Lower riskMedical device
Boston Scientific Corporation recalls Flexima Duodenal Bend Biliary Stent with Delivery System, 7F (2.3mm) x7cm, Material Number M00539210
Boston Scientific recalls Flexima Duodenal Bend Biliary Stent with Delivery System due to potential packaging seal defects. Affected units include specific model and lot numbers. Consumers should contact for details.
Boston ScientificDec 26, 2018 - UnratedMedical device
Varian Medical Systems, Inc. recalls Eclipse(TM) Treatment Planning System with Proton Convolution Superposition algorithm license only The Eclipse
Varian recalls Eclipse Treatment Planning System with Proton Conv: incorrect water equivalent range calculations for non-square CT images may affect proton therapy treatment planning.
VarianDec 26, 2018 - Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls LOPERAMIDE HCL TABLETS USP, 2 mg, ANTI-DIARRHEAL, 24 caplets per carton, OTC, Distributed by Drug Mart-Food Fair Medina
Sun Pharmaceutical recalls 24-capsule loperamide tablets due to inconsistent labeling between front and side panels showing 24 vs 12 caplets.
Sun PharmaceuticalDec 26, 2018 - Lower riskDrug
Glenmark Pharmaceuticals Inc., USA recalls Estradiol Vaginal Inserts, USP, 10 mcg, Rx only, packaged in a) 8 count (NDC 68462-711-71) and b) 18 count (NDC
Glenmark Pharmaceuticals recalls Estradiol Vaginal Inserts (10 mcg) due to customer reports of plunger malfunction in applicators. Affected units have specific NDC numbers and batch dates.
GlenmarkDec 26, 2018 - Use cautionMeat & poultry
Jennie-O Turkey Store Sales, Inc. Recalls Raw Ground Turkey Products due to Possible Salmonella Reading Contamination
Jennie-O recalls raw ground turkey products from Oct 2018 due to possible Salmonella Reading contamination. Consumers should not consume recalled items and cook turkey to 165°F to prevent illness.
Jennie-ODec 21, 2018 - Use cautionVehicle
KENWORTH T370 (2019) recall — Power Train
PACCAR recalls 2019 Kenworth T370 trucks with possible unintended movement causing crashes. Owners must update transmission control module free of charge by February 23, 2019.
PACCARDec 21, 2018 - Use cautionVehicle
HARLEY-DAVIDSON XG500 (2019) recall — Service Brakes, Hydraulic
Harley-Davidson recalls 2016-2019 XG500/XG750/XG750A motorcycles due to brake calipers corroding in coastal areas, causing increased brake drag and crash risk. Owners get free brake caliper replacements.
Harley-DavidsonDec 21, 2018
Browse recalls
- Recalls by vehicle make & model
- Pet food recalls
- Drug shortages
- September 2026 recall report
- All monthly reports
83,513 recalls tracked · 71,991 explained in plain English · 10,968 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.