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
34,960 found- Lower riskMedical device
InfuTronix LLC recalls Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a
InfuTronix recalls Nimbus Administration Sets (REF HS-004) with specific lot numbers due to potential tube leakage during fluid administration. Affected units may cause medication or fluid leaks.
InfuTronixMay 28, 2019 - Use cautionMedical device
Bio-Detek, Inc. recalls ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)
Bio-Detek recalls ZOLL Pro-padz Liquid Gel Radiolucent devices with part numbers 8900-2105-01 and 8900-2106-01 due to potential incorrect electrode assembly, which may prevent defibrillation or pacing therapy.
Bio-DetekMay 28, 2019 - Use cautionMedical device
GN Otometrics recalls The ICS CHARTR EP 200
GN Otometrics recalls ICS CHARTR EP 200 devices due to risk of electrical shock from undergrounded surfaces. Affected models include various versions with specific part numbers.
GN OtometricsMay 28, 2019 - Lower riskMedical device
Medline Industries Inc recalls SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml - Product Usage: Medline Silicone Foley catheter is a
Medline recalls silicone foley catheters with loose silicone particulate that could cause blockage or injury. Affected models include DYND11553 lot 287181201. Contact for return instructions.
MedlineMay 28, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are
Zimmer Biomet recalls DVR Crosslock ePAK Screw Drivers with model 212000002 due to potential weak sterile packaging seals. Affected units include specific lot numbers from 2018-2023. Consumers should check their product for the model and lot numbers listed.
Zimmer BiometMay 28, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This
Siemens recalls certain SOMATOM go.Up CT scanners with specific software versions due to potential workflow interruptions and delays in patient scans. Affected units may require software updates to prevent diagnostic delays.
SiemensMay 28, 2019 - Lower riskMedical device
Maquet Cardiovascular Us Sales, Llc recalls Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model: VST66DF
Maquet recalls VOLISTA StandOP Surgical Lights with model VST66DF and specific serial numbers due to risk of cracked light head forks causing surgical site infections. Affected units include serial numbers 500040-500050, 500069.
MaquetMay 28, 2019 - Lower riskDrug
Novis PR, Inc. recalls Pecgen DMX Cough Suppressant Expectorant, Contains the same active ingredients as Trispec DMX, Sugar Free, Alcohol
Novis PR recalls Pecgen DMX cough suppressant due to incorrect dosage instructions for children under 12. The label mistakenly states children 6-2 years should take 1 tsp every 4 hours, but it should be 6-12 years. Consumers should check labels for specific lot numbers and contact Novis PR for guidance.
Novis PRMay 28, 2019 - UnratedDrug
Synthetopes Inc recalls Sn-d, l-Exametazime (Sn-d,l-HMPAO), Not for Direct Injection, Store Below 25 C, Synthetopes, Inc.
Synthetopes recalls Sn-d,l-Exametazime (not for direct injection) due to lack of processing controls. All remaining lots within expiry date are affected. No specific remedy provided in official notice.
SynthetopesMay 28, 2019 - Use cautionFood
Nexagen, LLC recalls ACID RAIN ASS KICKING FAT DESTROYER APOCALYPSE LABZ; 45 CAPSULES; 1 DIETARY SUPPLEMENT; UPC 6 11138 28792 0
Nexagen recalls 157 bottles of Acid Rain dietary supplement. The product contains insufficient Higenamine and mislabels ingredients like Cayenne Pepper.
NexagenMay 28, 2019 - Stop using nowConsumer product
Children's Sleep Sacks Recalled by Gildan Activewear Due to Violation of Federal Flammability Standard; Sold Exclusively at AmericanApparel.com (Recall Alert)
American Apparel's Baby Rib Collection children's sleep sacks fail flammability standards, risking burns. Consumers should stop using and get refunds/replacements via American Apparel.
American ApparelMay 28, 2019 - Lower riskFood
Deep Foods Inc recalls "DEEP***GOLDEN RAISINS***NET WT***198g/7oz***DEEP FOODS, INC. UNION, NJ 07083"
Deep Foods recalls 7oz, 14oz, and 28oz Golden Raisins due to undeclared sulfites. Consumers should check UPC codes for affected products.
Deep FoodsMay 27, 2019 - Lower riskMeat & poultry
Sikorski Sausages Co., Ltd. Recalls Meat and Poultry Sausage Products Produced without Benefit of Import Inspection
USDA FSIS recalls approximately 74 pounds of imported meat and poultry sausages produced without U.S. inspection. Consumers are urged not to eat these products and should discard or return them.
Sikorski SausagesMay 24, 2019 - Use cautionVehicle
LAND ROVER RANGE ROVER (2013) recall — Latches/Locks/Linkages
Land Rover recalls 2013 Range Rovers with faulty Keyless Vehicle Latch system that may open mid-drive, risking crashes. Owners must contact for free software update by July 18, 2019 deadline.
Land RoverMay 24, 2019 - Use cautionVehicle
FOREST RIVER SHASTA (2017) recall — Equipment
Forest River is recalling 2017 Shasta recreational trailers due to a risk of LP gas leaks from improperly installed gas lines that could cause fires. Owners should contact customer service for free repairs.
Forest RiverMay 24, 2019 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Service Brakes, Air
Blue Bird recalls 2016-2020 All American buses with dragging rear brakes that may cause ABS warnings, vehicle stops, or fire risks. Owners must contact Blue Bird for free brake repairs.
Blue BirdMay 24, 2019 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Service Brakes, Air
Blue Bird is recalling 2019 school buses with dragging brakes that may cause ABS warning lights, vehicle stops, and fire risk. Owners must contact Blue Bird for free brake repairs.
Blue BirdMay 24, 2019 - Use cautionVehicle
AIRSTREAM BASECAMP (2020) recall — Equipment
Airstream is recalling certain 2017-2020 Basecamp trailers due to missing tire placard information, which could lead to incorrect spare tire installation and affect vehicle control, increasing crash risk.
AirstreamMay 24, 2019 - Use cautionMedical device
Cook Inc. recalls Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm, 5FR/135cm, Catalog Number ASB5-35-135-6-4, REF Number
Cook Inc. recalls Advance Enforcer 35 Focal Force PTA Balloon Catheter due to balloons bursting below rated pressure, risking vessel injury or procedure delays. Affected units have specific lot numbers.
Cook Inc.May 24, 2019 - Lower riskMedical device
Teleflex Medical recalls Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm, Product Code 5-22512 2) EZ-ENDO 6.5 mm, Product Code 5-22513 3) EZ-ENDO 7.0 mm,
Teleflex Medical recalls Hudson RCI Sheridan EZ-ENDO tubes (6.0-8.5mm) due to reported disconnections from endotracheal tubes in rare cases. Affected lots listed in product details.
Teleflex MedicalMay 24, 2019 - Lower riskMedical device
Abbott Laboratories recalls ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are for the calibration of the ARCHITECT iSystem
Abbott recalls ARCHITECT BNP Calibrators due to stability drift causing inaccurate BNP test results. Affected units include specific lot numbers from July 2019 to January 2020. Consumers should contact Abbott for details.
AbbottMay 24, 2019 - Lower riskFood
Stagno's Bakery, Inc. recalls Stagno's Bakery, Inc., P009, Choc Chip Bagel, Case 32lbs. Count per Case 120 of wholesale frozen bagel dough / bulk .
Stagno's Bakery recalls wholesale frozen bagel dough (P009) due to potential E. Coli contamination. Consumers should avoid using this product to prevent foodborne illness.
Stagno's BakeryMay 24, 2019 - Lower riskFood
LAIRD SUPERFOOD INC recalls Performance Mushrooms product is dried mushroom blend of 4 different mushroom mycelial biomass powders cultured on
Laird Superfood recalls Performance Mushrooms due to incorrect iron labeling. The product claims 14 mg of iron, but contains only 14 mcg.
Laird SuperfoodMay 24, 2019 - Use cautionMeat & poultry
Blount Fine Foods Recalls Soup with Chicken Products Due to Possible Foreign Matter Contamination
Blount Fine Foods recalls chicken tortilla soup products from April 2019 that may contain plastic. Consumers are urged not to consume these items and should discard or return them.
Blount Fine FoodsMay 23, 2019 - Use cautionVehicle
AUDI Q3 (2018) recall — Exterior Lighting
Audi is recalling certain 2016-2018 Q3 models with LED headlights due to potential turn signal indicator failure, which may increase crash risk. Owners must contact Audi for free BCM updates.
AudiMay 23, 2019 - Use cautionVehicle
BMW X7 (2019) recall — Air Bags
BMW is recalling 2019 X7 models with potentially misaligned head air bags that could increase injury risk during deployment. Owners must contact BMW for free air bag inspection and repair.
BMWMay 23, 2019 - Use cautionVehicle
KEYSTONE FUZION (2020) recall — Electrical System
Keystone is recalling certain 2018-2020 Fuzion 429 recreational trailers due to a potential wiring harness damage that could cause fire. Owners should contact customer service for free repairs.
KeystoneMay 23, 2019 - Lower riskMedical device
Richard Wolf Medical Instruments Corp. recalls E-Line Cutting Electrode 11.5Fr Mono 0 degrees, Sterile. One electrode is placed in a plastic tray and then inserted
Richard Wolf recalls E-Line Cutting Electrode 11.5Fr Mono 0 degrees due to incorrect electrode in package. This may cause improper use during medical procedures. Affected units have product number 8416.0305.
Richard WolfMay 23, 2019 - Use cautionMedical device
Obalon Therapeutics Inc recalls Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen; Software version 02.00.00.0076 - Product Usage: The
Obalon Therapeutics recalls specific model 4300 Touch Dispenser units with software version 02.00.00.0076 due to touchscreen calibration issues that may prevent balloon inflation during use.
ObalonMay 23, 2019 - Lower riskMedical device
Anewmed Corporation recalls Various products which were contract sterilized.
Anewmed Corporation recalls various products that were contract sterilized due to insufficient packaging data supporting a 2-year shelf life. Consumers should check product numbers listed in the recall notice.
AnewmedMay 23, 2019
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