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
34,946 found- Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6 and RayStation 7, a stand-alone software treatment planning
RaySearch Laboratories recalls RayStation software versions 4.5 to 7 due to unsupported robust optimization for treatment plans. Affected users should contact for updates.
RaySearch LaboratoriesSep 21, 2018 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are
DePuy recalls certain CORAIL hip implants due to potential debris behind O-rings. Affected models include specific lot numbers for hip surgery instruments. Contact DePuy for details.
DePuySep 21, 2018 - Lower riskMedical device
Arrow International Inc recalls Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code
Arrow recalls AGB+ Multi-Lumen CVC Kits with inconsistent labeling of spring wire guide size. This may cause confusion in medical use but does not pose a safety risk.
ArrowSep 21, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds are sterile disposables
Zimmer Biomet recalls StageOne Hip cement spacer molds 431207 and 431209 due to potential mixing of 43mm and 51mm molds. These sterile medical devices could cause incorrect joint fitting if used improperly.
Zimmer BiometSep 21, 2018 - Lower riskMedical device
The Metrix Company recalls SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 4000mL, (legless) REF 66640 - Product Usage: For use in an
Metrix recalls SECURE EVA Dual Chamber Containers (REF 66640) for potential leaking during intravenous use. Affected units have lot numbers 66640-A2404 and 66640-A4324.
MetrixSep 21, 2018 - Lower riskDrug
Teva Pharmaceuticals USA recalls Clozapine Orally Disintegrating Tablets, 12.5 mg, 100-count bottles, Rx only, Teva Pharmaceuticals USA, Inc., North
Teva Pharmaceuticals recalls 12.5mg Clozapine orally disintegrating tablets due to failed disintegration test. Rx-only medication with specific lot number and expiration date.
Teva PharmaceuticalsSep 21, 2018 - Lower riskDrug
Dr. Reddy's Laboratories, Inc. recalls Nystatin and Triamcinolone Acetonide Cream, USP, 100,000 units/gm & 1 mg/gm, packaged in a) 15 g tube (NDC
Dr. Reddy's recalls Nystatin and Triamcinolone Acetonide Cream due to stability issues. Out of specification composition found during testing. Rx only products with specific lot numbers and expiration dates.
Dr. Reddy'sSep 21, 2018 - Lower riskFood
Victoria Gourmet, Inc. recalls Victoria Taylor's Seasonings - Blackening Rub, 6.4 oz., UPC: 666227015274, packaged in a glass jar with a lid
Victoria Gourmet recalls Blackening Rub seasoning due to incorrect labeling on glass jars. Consumers should check UPC 666227015274 for affected products.
Victoria GourmetSep 21, 2018 - Stop using nowFood
Lloyd'S Ice Cream Inc recalls Lic's REESE'S OREO, ONE QUART (946 mL), packed in Plastic quart container
Lloyd's Ice Cream recalls Lic's Reese's Oreo Ice Cream because the label fails to declare peanuts, posing a risk to those with allergies.
Lic'sSep 21, 2018 - Stop using nowConsumer product
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Woodcraft Recalls Clip-On Adapters for Motorcycle Handlebars Due to Crash Hazard
Woodcraft recalls clip-on handlebar adapters due to cracking crash hazard. Stop using immediately and contact Woodcraft for a free replacement.
WoodcraftSep 21, 2018 - Stop using nowMeat & poultry
Zweigle's Inc. Recalls Olive Loaf Pork Products due to Sodium Nitrite Levels in Excess of Regulatory Limit
USDA FSIS recalls 6,082 pounds of Zweigle's olive loaf pork products due to sodium nitrite levels exceeding regulatory limits. Consumers urged not to consume and dispose of items.
Zweigle'sSep 20, 2018 - Use cautionVehicle
SCION TC (2016) recall — Service Brakes, Hydraulic
Toyota recalls Scion TC (2016) vehicles with optional TRD brake kits due to brake hose failure risk. Replace with standard brake kit free of charge.
ToyotaSep 20, 2018 - Use cautionVehicle
NEWMAR DUTCH STAR (2019) recall — Service Brakes, Hydraulic
Newmar is recalling 2019 Dutch Star motorhomes with brake pedal assembly that may catch on dash, preventing full release. This fails federal brake safety standards and requires free brake adjustment cable repair.
NewmarSep 20, 2018 - Use cautionVehicle
KEYSTONE FUZION (2019) recall — Service Brakes, Electric
Keystone is recalling 2016-2019 Fuzion trailers due to brake wiring that may damage and reduce braking ability. Owners should contact customer service for free repairs.
KeystoneSep 20, 2018 - Use cautionVehicle
BMW 530E (2019) recall — Equipment
BMW recalls 2019 530e models with faulty charging cables that may cause fire or shock. Owners must have cable inspected and replaced free by dealers.
BMWSep 20, 2018 - Lower riskMedical device
AS Software, Inc. recalls AS-OBGYN Information System version 7.824.x
AS Software recalls version 7.82: Software changes without testing may cause ultrasound measurements to be inaccurate. Affected users should verify their software version and contact support.
AS SoftwareSep 20, 2018 - Lower riskMedical device
Micro-Tech (Nanjing) Co., Ltd. recalls Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) -
Micro-Tech recalls JUMBO ALLIGATOR biopsy forceps with incorrect grasping forceps in the box. Consumers should check product details to avoid using the wrong tool.
Micro-TechSep 20, 2018 - Use cautionMedical device
Maquet Datascope Corp - Cardiac Assist Division recalls Cardiosave Hybrid IABP, Part Number 0998-00-0800-53
Maquet recalls Cardiosave Hybrid IABP devices with part number 0998-00-800-53 for potential therapy interruption at high altitudes above 3200 ft.
MaquetSep 20, 2018 - Lower riskDrug
Teva Pharmaceuticals USA recalls Clonazepam Orally Disintegrating Tablets USP, 2 mg., 60-count carton. RX only. Teva Pharmaceuticals USA, INC. North
Teva Pharmaceuticals recalls 2mg Clonazepam orally disintegrating tablets due to water content failure in stability testing. This affects RX-only products with specific lot numbers.
Teva PharmaceuticalsSep 20, 2018 - UnratedDrug
Pfizer Inc. recalls Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC.
Pfizer recalls 500-tablet Glipizide XL 5mg bottles (Rx only) due to manufacturing deviations. Affected lots were used in final production. Consumers should contact Pfizer for details.
PfizerSep 20, 2018 - Stop using nowDrug
Pfizer Inc. recalls Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira,
Pfizer recalls Meropenem for Injection (1g/vial) due to potential loss of container integrity, risking contamination. Affected lots manufactured for Hospira in Lake Forest, IL. Stop using immediately.
PfizerSep 20, 2018 - Stop using nowFood
Tarry Medical Products, Inc. recalls Product comes in a plastic bag which is labeled as follows: DandleLION MEDICAL DandleLION KISSES ORAL USE ONLY SINGLE
Tarry Medical Products recalls DandleLION Kisses oral solution due to microorganism contamination. Check lot F17272 for details.
DandleLION MedicalSep 20, 2018 - Use cautionFood
Artisan Baking Company, LLC. recalls Village Baker SPECIALTY ARTISAN BREADS CINNAMON CHIP SOURDOUGH. The product is whole sliced loaves packed in clear
Artisan Baking Company recalls Village Baker Cinnamon Chip Sourdough bread due to undeclared milk and soy. Check your label for allergen info.
Village BakerSep 20, 2018 - Use cautionFood
Lamb Weston Inc recalls Formed Hash Brown Patties, packaged in cardboard trays covered with plastic film, frozen products. The following brands
Lamb Weston recalls hash brown patties from Brookshire's, Market Pantry, Breakfast, and Stater Bros. due to possible small plastic fragments. Consumers should check UPCs and dates to identify affected products.
Lamb WestonSep 20, 2018 - Stop using nowConsumer product
Weeplay Kids Recalls Children's Coveralls Due to Choking Hazard
ED by Ellen DeGeneres recalls infant coveralls with detachable bunny applique that can cause choking. Return to store for full refund.
ED by Ellen DeGeneresSep 20, 2018 - Stop using nowConsumer product
Titan Recalls Weight Lifting Safety Straps Due to Injury Hazard (Recall Alert)
Titan recalls weight lifting safety straps with model numbers 24T3STRAP, 26T2STRAP, 30X3STRAP, 36T3STRAP, X2STRAP24, 24X3STRAP, 36X3STRAP due to potential strap failure causing weights to fall and injure users.
TitanSep 20, 2018 - Stop using nowConsumer product
Kaz Recalls Stinger Insect Zappers Due to Shock Hazard
Kaz recalls Stinger BK series insect zappers (models BK110v3, BK310v3, BK510v3) due to risk of shock from detached insect kill grid. Consumers must stop using, unplug, and return for refund.
KazSep 20, 2018 - Use cautionMeat & poultry
Cargill Meat Solutions Recalls Ground Beef Products due to Possible E. coli O26 Contamination
Cargill recalls ground beef products from June 2018 due to possible E. coli O26 contamination. Consumers are urged not to consume these products and should discard or return them to the place of purchase.
CargillSep 19, 2018 - Use cautionVehicle
LIVIN' LITE CAMPLITE (2018) recall — Structure
Livin' Lite is recalling certain 2017-2019 CampLite travel trailers due to a risk of trailer separation from tow vehicles, which could increase crash risk. Owners should contact customer service for free repairs.
Livin' LiteSep 19, 2018 - Use cautionVehicle
WESTERN STAR 4900 (2019) recall — Tires
Daimler Trucks North America recalls 2019 Western Star 4900 trucks with certain Bridgestone tires (date codes 2418-2518) due to risk of rapid air loss causing crashes. Owners must have tires inspected and replaced free.
Western StarSep 19, 2018
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