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- Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) - Product Usage: intended to be used for the
Baxter recalls SIGMA Spectrum Infusion Pump (Version 6) due to potential software error during programming. Affected units may require correction to prevent administration issues.
BaxterNov 23, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in vitro diagnostic use in the quantitative
Siemens Healthcare recalls Atel:lica GGT reagents due to potential low repeatability in lab tests. Affected lots may show inconsistent results on some analyzers. No remedy specified in recall notice.
Siemens HealthcareNov 23, 2020 - Use cautionMedical device
Covidien Llc recalls Covidien TA Auto Suture Vascular Loading Unit with DST Series Technology 30 mm- V3. Intended for abdominal,
Covidien recalls TA Auto Suture Vascular Loading Unit V3 (model TA30V3L) with specific lot numbers due to potential damaged internal components that may cause incomplete staple formation, leading to bleeding, infection, or other complications during surgery.
CovidienNov 23, 2020 - Lower riskMedical device
B Braun Medical, Inc. recalls APEX Compounding System Control Panel Module, REF: 601237, Product Code AX1000 - Product Usage: intended for
B Braun recalls APEX Compounding System Control Panel Module (AX1000) with software version 1.0.5.57 or earlier. The system may not detect air bubbles exceeding 3% of the ordered volume, risking inaccurate drug compounding.
B BraunNov 23, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls Revolution CT ES - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography
GE Healthcare recalls Revolution CT ES X-ray scanners due to potential protocol errors causing patient safety risks. Affected units have specific model and serial numbers. Consumers should contact GE for details.
GE HealthcareNov 23, 2020 - Lower riskMedical device
Fresenius Medical Care Holdings, Inc. recalls Naturalyte Liquid Acid concentrate bottles, Product Code 08-2201-5 - Product Usage: used in conjunction with Fresenius
Fresenius Medical Care recalls Naturalyte Liquid Acid concentrate bottles (Product Code 08-2201-5) due to sodium level deviations that could affect dialysis treatment safety.
Fresenius Medical CareNov 23, 2020 - UnratedDrug
Ascend Laboratories LLC recalls Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, packaged as a) 100 ml (when mixed) bottle, NDC 67877-544-88; b)
Ascend Laboratories recalls Cephalexin oral suspension (125mg/5mL) due to unidentified impurities in some lots. Products may not meet safety standards.
Ascend LaboratoriesNov 23, 2020 - UnratedFood
Shenandoah Growers, Inc. recalls Organic fresh cut basil packaged in plastic clamshell containers The Fresh Market Organic Basil NET WT 0.5oz (14g),
Shenandoah Growers recalls organic fresh cut basil products due to possible Cyclospora contamination. Consumers should check UPCs listed to determine if their product is affected.
Shenandoah GrowersNov 23, 2020 - Lower riskFood
Whole Foods Market recalls Whole Foods Market Popcorn Chicken Shaker with Sweet Chili Variable weight sold by lb. Packed For Whole Foods Market
Whole Foods Market recalls Popcorn Chicken Shaker with Sweet Chili due to undeclared shrimp allergen from mislabeling. Consumers should check product dates and avoid if allergic to shrimp.
Whole Foods MarketNov 23, 2020 - Lower riskFood
PRAIRIE FARMS recalls Prairie Farms Premium Flavored Chocolate Milk, 1 gallon, UPC 72730-26110
Prairie Farms recalls 1-gallon chocolate milk with undeclared egg. Consumers should check UPC 72730-26110 and avoid use due to potential allergen risk.
Prairie FarmsNov 23, 2020 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Chicken and Beef Samosa Products Containing Pastry Ingredients That Have Been Recalled Due to Misbranding
FSIS public health alert: Taza chicken and beef samosas may contain undeclared milk, a known allergen. Consumers urged not to consume these products due to misbranding.
TazaNov 21, 2020 - Lower riskFood
Dole Fresh Vegetables Inc recalls Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt
Dole Fresh Vegetables Inc recalls organic romaine hearts due to pathogenic non-O157 E. coli STEC detected in routine sampling. Consumers should avoid using these products.
DoleNov 21, 2020 - Use cautionVehicle
VOLKSWAGEN TIGUAN (2018) recall — Seat Belts
Volkswagen recalls 2018 Tiguan LWB vehicles with potentially torn front seat belts that may not restrain occupants during crashes, increasing injury risk. Owners can get free replacements.
VolkswagenNov 20, 2020 - Use cautionVehicle
LINCOLN AVIATOR (2021) recall — Steering
Ford is recalling 2021 Lincoln Aviators with potentially improperly manufactured steering knuckles that could fracture, reducing steering control and increasing crash risk. Owners will receive free inspections and replacements.
FordNov 20, 2020 - Use cautionVehicle
HONDA PILOT (2021) recall — Tires
Honda is recalling 2021 Pilot vehicles with specific Continental CrossContact LX Sport tires due to potential sidewall breaks causing sudden air loss or loss of vehicle control. Owners must have tires with DOT serial numbers A376 D3K9 2920 and mold numbers S-421920/S-421921.
HondaNov 20, 2020 - Use cautionVehicle
TRIPLE E UNITY (2020) recall — Equipment
Triple E is recalling 2020 Unity motorhomes with potential tail light failure due to water tank bracket shifting. Owners must contact customer service for free bracket installation.
Triple ENov 20, 2020 - Use cautionVehicle
NEWMAR DUTCH STAR (2020) recall — Equipment
Newmar recalls 2020 Dutch Star motorhomes with Dometic cooking stoves that may leak gas, risking fire. Owners must contact customer service for free repair kit installation.
NewmarNov 20, 2020 - Use cautionMedical device
Haag-Streit USA Inc recalls Haag Streit Surgical Floor stands FS 2-11 (Ref no. 615H511) and FS 2-15 (Ref no. 615H515) in combination with the
Haag-Streit recalls surgical floor stands FS 2-11 and FS 2-15 with specific software versions that may cause eye injury during use in ophthalmology. Affected units have serial numbers starting from 1001.
Haag-StreitNov 20, 2020 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of
Zimmer Biomet recalls Spinal Rod Cutter (item 00392500200) due to potential fracture during surgical use. Affected units may cause injury if not handled properly.
Zimmer BiometNov 20, 2020 - Use cautionMedical device
Maquet Cardiovascular Us Sales, Llc recalls HLS Set Advanced Model Name: BEQ-HLS 5050 USA; HLS Set Advanced 5.0, Product Code/Part Number: 70105.2797 - Product
Maquet recalls HLS Set Advanced 5.0 models with product code 70105.2797 due to sterility barrier breaches that could cause infections during cardiac surgery.
MaquetNov 20, 2020 - Use cautionMedical device
Ortho-Clinical Diagnostics, Inc. recalls enGen Laboratory Automation System, enGen Track System, Catalog Number ENGEN - Product Usage: intended for use in the
Ortho-Clinical recalls enGen Lab Automation Systems with software versions 4.6 and below due to risk of incorrect patient sample labeling, potentially leading to harmful medical interventions.
Ortho-ClinicalNov 20, 2020 - Lower riskDrug
SCA Pharmaceuticals recalls Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205
SCA Pharmaceuticals recalls Fentanyl 250 mcg/5mL injections due to subpotency issues from stability testing. Affected lots expire by Dec 2020. Contact for details.
SCA PharmaceuticalsNov 20, 2020 - Lower riskDrug
Novocol Pharmaceutical of Canada, Inc. recalls Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor), packaged in cartons of 50 cartridges (1.7
Novocol recalls Scandonest 3% Plain cartridges due to labeling errors. This may cause confusion with other products. Check your carton for batch numbers and contact Novocol for details.
NovocolNov 20, 2020 - Lower riskDrug
Complete Pharmacy and Medical Solutions, LLC. recalls HUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection.
Complete Pharmacy recalls HUMAN CHORIONIC GONADOTROPIN 1,250 IU vials due to lack of potency testing. Affected lots were manufactured in Miami Lakes, FL.
Complete PharmacyNov 20, 2020 - Stop using nowFood
J F C International Inc recalls YAGUMO AMANATTO GIFT BOX 6P 6/19.01 OZ JAN Code: 49 03089 39050 4 Imported by JFC International Inc. Los Angeles, CA
JFC International recalls Yagumo Amanatto Gift Boxes due to potential mold contamination. Check your JAN code and lot details.
YagumoNov 20, 2020 - Lower riskFood
Out of the Kitchen, LLC recalls Chef Mitch Maier's Black Garlic Ketchup. Net Wt. 19 oz. (538g). UPC 8 60248-00254 5.
Out of the Kitchen recalls Chef Mitch Maier's Black Garlic Ketchup due to mold growth before the Best By date. Consumers should check lot codes and discard if expired.
Out of the KitchenNov 20, 2020 - Lower riskFood
Riverside Natural Foods, Ltd. recalls Good & Gather Banana Chocolate Chip Date & Nut Bars, UPC 0 85239-04216 8. 5-1.6 oz (45g) Bars. Net Wt. 8oz (225g). DIST
Riverside Natural Foods recalls Good & Gather Banana Chocolate Chip Date & Nut Bars due to undeclared almonds. Consumers should check UPC 085239042168 for affected items.
Riverside Natural FoodsNov 20, 2020 - Use cautionVehicle
THOR MOTOR COACH FOUR WINDS (2021) recall — Equipment
Thor Motor Coach is recalling certain 2021 Four Winds motorhomes with Dometic 3-burner stoves due to a potential gas leak causing fire risk. Owners must have the saddle valve bolt overtightened.
Thor Motor CoachNov 19, 2020 - Lower riskMedical device
Lidco Ltd recalls CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium
Lidco recalls CM 50-001-01 Injectate Kit due to incorrect expiration date on labeling. This accessory for LiDCOunity v2 Monitor may expire before use, potentially causing safety issues.
LidcoNov 19, 2020 - Lower riskMedical device
Philips North America, LLC recalls Emission Computed Tomography System Image Process System - Product Usage: intended for general Nuclear Medicine imaging
Philips recalls certain Emission Computed Tomography Image Process Systems due to a software defect that may cause image misdiagnosis and incorrect patient treatment. Affected models include 882310, 882311, and 882313.
PhilipsNov 19, 2020
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83,613 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.