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
35,069 found- Stop using nowDrug
Celebrate Today recalls RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
Celebrate Today recalls 400mg RED MAMMOTH capsules sold with undeclared sildenafil and tadalafil. These unapproved drugs may cause serious health risks. Consumers should stop using and consult a doctor.
Celebrate TodayFeb 8, 2022 - Stop using nowDrug
Your Favorite Shop recalls THE RED PILL, EXTRA STRENGTH capsules, 800 mg, packaged in 10-count blisters packaged in a carton, ASIN B0847BSQQ5,
Your Favorite Shop recalls Red Pill Extra Strength 800mg capsules (ASIN B0847BSQQ5) due to undeclared tadalafil, an unapproved drug ingredient. Consumers should stop using immediately.
Your Favorite ShopFeb 8, 2022 - UnratedDrug
ABC Sales 1 Inc recalls MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191.
ABC Sales 1 Inc recalls MAC DADDY RED Capsules (10-count blisters) due to unapproved ingredients. These capsules contain undeclared tadalafil and sildenafil, which are FDA-approved for male sexual enhancement but were not properly approved for this product.
ABC Sales 1 IncFeb 8, 2022 - Stop using nowFood
Jan Fruits, Inc. recalls Taiwan Best Quality Enoki Natural Mushrooms, Premium 200g/7.5 oz. clear plastic package. 50 pcs per box. Manufacturer:
Jan Fruits recalls Taiwan Best Quality Enoki Natural Mushrooms due to Listeria monocytogenes detected in samples. Consumers should check for clear plastic packaging and 200g/7.5oz boxes with 50 pieces per box.
Jan FruitsFeb 8, 2022 - Use cautionMedical device
B Braun Medical Inc recalls PERFUSOR SPACE - US VERSION. Intended Use: syringe infusion pump that can be used to configure customized, tailor-made
B Braun recalls US version PERFUSOR SPACE infusion pumps with serial numbers 633299-633318 due to potential infusion errors. Affected units may cause delays, overinfusion, or underinfusion of medication.
B BraunFeb 7, 2022 - Lower riskMedical device
Brius Technologies Inc. recalls Brius Patient Specific Brackets (components in a set of custom metal orthodontic devices); BRIUS , RX Only,
Brius recalls custom orthodontic brackets sold without completing standard design controls. These devices may not be safe for use until proper testing is done.
BriusFeb 7, 2022 - Lower riskMedical device
Philips North America, LLC recalls The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following
Philips recalls autoclavable temperature probes with model numbers 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641. The recall involves updated cleaning instructions to prevent improper disinfection.
PhilipsFeb 7, 2022 - Stop using nowDrug
Teligent Pharma, Inc. recalls Erythromycin Topical Gel USP, 2%, Net Wt 30 g tube, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310,
Teligent Pharma recalls 30g Erythromycin Topical Gel USP 2% tubes due to impurities that could cause serious injury. Rx-only product manufactured in Buena, NJ. Check NDC 63739-053-66 for affected lots.
Teligent PharmaFeb 7, 2022 - Use cautionDrug
Tsm Brands LLC recalls Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1PT) 473 ML bottle, Distributed by: TSM Brands LLC, 540 Equinox Ln,
TSM Brands LLC recalls Luxury 70% Isopropyl Alcohol bottles due to undeclared ethyl alcohol. Check lot numbers and UPC for details.
LuxuryFeb 7, 2022 - Lower riskDrug
RISING PHARMACEUTICALS recalls Methylphenidate Hydrochloride Chewable Tablets, 2.5 mg, 100-count bottle, Rx Only, Manufactured for: Rising
Rising Pharmaceuticals recalls 2.5 mg chewable methylphenidate tablets due to size variation in some tablets. This may affect safety and requires verification of product details.
Rising PharmaceuticalsFeb 7, 2022 - Use cautionDrug
SUN PHARMACEUTICAL INDUSTRIES INC recalls Chlorthalidone Tablets USP 25 mg, Rx Only, 100 Tablets, Sun Pharma, Mfg. by: Fontida Bio Pharm Inc., 1100 Orthodox St.
Sun Pharma recalls 25mg Chlorthalidone tablets with stainless steel particles. Foreign matter in tablets may cause injury. Stop using and contact for return.
Sun PharmaFeb 7, 2022 - Lower riskFood
American Gourmet recalls American Gourmet Saladitos (Dried Salted Plums) 1.5 oz. package UPC: 1578600104
American Gourmet recalls 1.5 oz. Saladitos dried salted plums (UPC 1578600104) due to high lead levels detected in samples. Consumers should check product details and contact the company for instructions.
American GourmetFeb 7, 2022 - UnratedFood
Mohammad Mayha recalls Jaguar Power Honey packaged in a gold paper box with black writing, 12 sachets per box UPC 3553314142227
Jaguar Power Honey (12 sachets) with UPC 3553314142227 recalled due to hidden drug ingredient. Consumers should check packaging for gold box with black writing.
Mohammad MayhaFeb 7, 2022 - Lower riskFood
Garden-Fresh Foods, Inc. recalls Weis Original Potato Salad, Net Wt 64 oz (4 lb) 1.81kg. UPC 41497-19347. Keep Refrigerated
Garden Fresh Foods recalls Weis Original Potato Salad (64 oz) due to undeclared milk. This may cause allergic reactions in sensitive individuals. Check UPC 41497-19347 for affected products.
Garden Fresh FoodsFeb 7, 2022 - UnratedFood
Candies Tolteca recalls Tolteca Saladitos con Chile Limon, Dried Plums with Chili & Lemon; Net Wt. .15 oz. (42.5g) packaged in a clear
Tolteca recalls Saladitos con Chile Limon and Dried Plums with Chili & Lemon due to potential high lead levels in firm dried salted plums. Consumers should check packaging for UPC 704927600700 and stop using if concerned.
ToltecaFeb 7, 2022 - Use cautionVehicle
CADILLAC XT6 (2022) recall — Service Brakes, Hydraulic
General Motors recalls 2022 Cadillac XT6 vehicles with missing brake fluid warning labels that could lead to brake failure and crashes.
CadillacFeb 6, 2022 - UnratedFood
Rojas Inc. recalls LUPAG brand Plain Dried Salted Plums, net wt. 0.5oz, pre-priced at $.99 packaged in transparent poly bags sealed with a
Rojas Inc. recalls LUP: Plain Dried Salted Plums (0.5oz) due to elevated lead levels. Consumers should avoid use until further notice.
LUPAGFeb 6, 2022 - Use cautionVehicle
KZRV SONIC (2021) recall — Equipment
KZRV is recalling 2021-2022 Sonic trailers due to potential gas leaks from cracked quick disconnect fittings, which could cause fire if ignited. Owners must contact KZRV for free replacement.
KZRVFeb 5, 2022 - Lower riskMedical device
Cytocell Ltd. recalls TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA
Cytocell recalls TCL1 Breakapart Probe for possible unexpected DNA signals. Learn if you have the affected product and what to do.
Cytoc:ellFeb 4, 2022 - Lower riskMedical device
Philips North America LLC recalls Philips, REF M5071A, Adult. Smart PADS CARTRIDGE, 8+ years FOR USE WITH HEARSTART HS1 DEFIBRILLATORS
Philips recalls adult Smart Pads cartridges for HEARSTART HS1 defibrillators due to potential gel separation that could reduce pad effectiveness. Affected units sold since 2:00 PM on 2023-08-01.
PhilipsFeb 4, 2022 - Use cautionMedical device
ev3 Inc. recalls Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For use in peripheral
Medtronic recalls its TurboHawk Plus 6F directional atherectomy system for small vessel use due to tip detachment risk. Affected units have catalog number THP-S and GTIN 007630:00402419.
ev3Feb 4, 2022 - UnratedDrug
CooperSurgical, Inc recalls PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white
CooperSurgical recalls PARAGARD T380A intrauterine copper contraceptives due to non-sterility risk. One unit per carton with insertion tube and white rod is affected. No remedy specified in official notice.
CooperSurgicalFeb 4, 2022 - Lower riskDrug
Professional Disposables International, Inc. recalls Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab, 3.15% w/v and 70% v/v, packaged as a) One Swab, 0.034
Recalled Prevantics swabs (3.15% chlorhexidine gluconate) due to uncertainty in test method validation. Check NDC 10819-1080-1 or 10819-1080-2 for affected lots.
Professional Disposables InternationalFeb 4, 2022 - UnratedDrug
Junp Hydration LLC recalls MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a carton, UPC 8 48998 00091 2,
Junp Hydration recalls MegMan Performance Booster capsules due to undeclared tadalafil, an unapproved drug ingredient. This product was marketed without FDA approval and poses health risks.
Junp HydrationFeb 4, 2022 - Stop using nowFood
GOLDEN MEDAL MUSHROOM INC recalls Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is
Golden Medal Mushroom Inc. recalls Enoki mushrooms (UPC 6 953150 100684) due to Listeria monocytogenes detected in samples. Consumers should check packaging for green text and blue code 300511.
Golden Medal MushroomFeb 4, 2022 - Use cautionVehicle
BMW 128I (2013) recall — Engine And Engine Cooling
BMW recalls certain 2008-2013 1 Series and 3 Series vehicles due to PCV valve heater overheating that could cause fire while driving or after parking.
BMWFeb 3, 2022 - Stop using nowVehicle
FREIGHTLINER BUSINESS CLASS M2 (2020) recall — Service Brakes, Air
Freightliner recalls 2020-2022 Business Class M2 trucks due to cracked brake drums. Check your VIN and contact DTNA for remedy details.
FreightlinerFeb 3, 2022 - Lower riskMedical device
Terumo Cardiovascular Systems Corp recalls Cardiovascular Procedure Kit catalog # 76645 & 73806
Terumo recalls two cardiovascular procedure kits (catalog #76645 & 73806) due to potential shipping damage. Affected kits may have packaging issues that could impact use.
TerumoFeb 3, 2022 - Lower riskMedical device
Volcano Corp recalls MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller), Part Numbers: 300002018101, 300002018102, used
Volcano Corp recalls MM-TSM touch screen modules used with IVUS systems that may crack, causing non-functionality. Affected units have specific part numbers and require replacement of protective beams.
Volcano CorpFeb 3, 2022 - Lower riskMedical device
Abbott Laboratories, Inc recalls Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended
Abbott recalls Alinity s System software version 2.8.0 (serials AS1001-AS1368) due to wash buffer error causing potential inaccurate test results. This is an in vitro diagnostic device.
AbbottFeb 3, 2022
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