Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,301–11,350 of 15,364
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Chocolate Bars Cookie Butter UPC 755003858751Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Micro Dose Strawberry Kiwi UPC 755003861409Toxic levels of muscimol
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: a) MINOR BREAST, Pack Number DYNJ908104B; b) PLASTIC MAJOR, Pack Number DYNJ908106B; c) ABDOMINOPLASTY W/LIPO SDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Mega/Extreme Dose Blue Razz Euphoria UPC 810133320346Toxic levels of muscimol
- Class II
Drug Recall · June 27, 2024
Zydus Pharmaceuticals (USA) Inc
Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India, NDC 16714-165-01.Presence of particulate matter: glass
- Class II
Medical Device Recall · June 27, 2024
Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250. Capio SLIM Suture Capturing Devices are used by physicians to facilitate the consistent placement of sutures during open surgical proceduSome lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Micro Dose Grape Lemonade UPC 755003861584Toxic levels of muscimol
- Class II
Food Recall · June 27, 2024
Lipari Foods Operating Company, LLC.
Premo King Club Footlong 11.5oz, clear plastic, UPC 612510094259, 4 retail packages per wholesale casePotential contamination with Salmonella
- Class II
Medical Device Recall · June 27, 2024
Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVDTheir is a potential for high background and off-target staining when using the monoclonal primary antibody which can result in false positive results.
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Chocolate Bars Cookies & Cream UPC 755003858782Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Mega/Extreme Dose Watermelon Wonderland UPC 810133320421Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Micro Dose Sour Peach Apple UPC 755003861386Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Infused Cones Double Chocolate Chip UPC 810133320001Toxic levels of muscimol
- Class II
Medical Device Recall · June 27, 2024
LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Chocolate Bars Birthday Cake UPC 75503858867Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Infused Cones Mint Chocolate Chip UPC 810133320049Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Mega/Extreme Dose Lucid Lemon Lime UPC 810133320360Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Chocolate Bars Cinnamon Bar UPC 755003858836Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Mega/Extreme Dose Peach Paradise UPC 810133320384Toxic levels of muscimol
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Gummies - Micro Dose Hawaiian Punch UPC 755003861850Toxic levels of muscimol
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: MTHZ GYN LAPAROSCOPY, Pack Number DYNJ909739Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Class I
Food Recall · June 27, 2024
Diamond Shruumz Infused Cones Cookies and Cream UPC 810133320025Toxic levels of muscimol
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: a) ANESTHESIA CIRCUIT-LF, Pack Number DYNJAA0311C; b) ANESTHESIA CIRCUIT-LF, Pack Number DYNJAA0323C; c) ANESTHESDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: MERCY TIFFIN C-SECTION, Pack Number DYNJ909732Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Class II
Medical Device Recall · June 27, 2024
Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner, NA/6000-00-00L; Arctic Sun Stat EU UK/600001; Arctic Sun Stat Taiwan/600006; Arctic SIf temperature management system fails to reach correct target water temperature while device is operating in patient control mode, due to sudden patient temperature changes/interruption in water flow/blockage of air flow by an obstruction or dirty filter, then system may not alert, and alarm absence may lead to hypothermia or hyperthermia, so a software update will be released to correct issue.
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: a) BAPTIST FLOYD BRONCHOSCOPY, Pack Number DYKE1456D; b) ENT MINOR, Pack Number DYNJ908099B; c) HEAD & NECK, PackDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: NICU ADMIT KIT, Pack Number DYKA1014GDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Class II
Medical Device Recall · June 27, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline convenience kits containing semi-rigid suction liners labeled as follows: ANES TURNOVER KIT-LF, Pack Number DYNJAA10338JDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
- Unclassified
Consumer Product Recall · June 27, 2024
Shenzhen Baseus Technology Co. Ltd., of China
Baseus Magnetic Wireless Charging Power BanksThe lithium-ion battery in the power banks can overheat, posing a fire hazard.
- Unclassified
Consumer Product Recall · June 27, 2024
Dania Furniture, of Boise, Idaho
Hayden BookcaseThe recalled bookcase is unstable if it is not anchored to the wall, posing tip-over and entrapment hazards that can result in death or serious injuries to children.
- Unclassified
Consumer Product Recall · June 27, 2024
At Home Procurement Inc., of Dallas, Texas
Tie Dye Fur Toy Trunk Storage ChestsThe toy trunk storage chests do not contain a lid support feature or ventilation holes, posing entrapment and suffocation hazards.
- Unclassified
Consumer Product Recall · June 27, 2024
RECREATIONAL EQUIPMENT INC. (REI), of Sumner, Washington
Co-op Cycles REV 12-, 16-, or 20-inch Kid's Bicycles with training wheels (all model years 2022-2024)The training wheel assembly knob can loosen and detach from the bicycle, posing fall and injury hazards to the riders.
- Class II
Medical Device Recall · June 26, 2024
Siemens AG/Siemens Healthcare GmbH
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24JPCertain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD
DVOT SARS-CoV-2 & RSV &MP &ADV & FIu A/B Antigen Combo Test Kit, Model Number ACT01The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.
- Class II
Drug Recall · June 26, 2024
Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules, 30-count blister card, Rx only, MFG: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-120CGMP Deviations: Out of specification for dissolution
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD
DVOT SARS-Cov-2 &Influenza A+B Antigen Combo Test Kit, Model Number FAT01The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.
- Class III
Drug Recall · June 26, 2024
Dr. Reddy's Laboratories, Inc.
Sevelamer Carbonate for Oral Suspension 0.8g packets, packaged in 90 packets per container, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India NDC 43598-478-90Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
ENT RES, 100 ML, Non-Sterile W CLAMP & FEMALE LUER, Product Code 68-2231-28Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 50mL, FS, Product Code 21-7301-24JPCertain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Drug Recall · June 26, 2024
Blemfree All Day Lotion (salicylic acid 0.5% w/w), packaged in a) 1 oz. 29 ML tube NDC:53228-003-01 b) 4 OZ 118ML plastic bottle, UPC 7 01450 90008 6, NDC # 53228-002-01, Equibal Labs, IncCGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
- Class II
Medical Device Recall · June 26, 2024
CADD Medication Cassette Reservoir, 50mL, Product Code 21-7001-24Certain CADD Medication Cassette Reservoirs may exhibit a weakened weld joint between the medication bag and tubing due to a production equipment malfunction. This could result in a medication leakage.
- Class II
Medical Device Recall · June 26, 2024
Siemens AG/Siemens Healthcare GmbH
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.
- Class II
Drug Recall · June 26, 2024
Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.CGMP Deviations and Presence of Particulate Matter: Glass
- Class II
Drug Recall · June 26, 2024
Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches containing 60 capsules, Distributed by: Guru Inc., 4370 Lawrenceville Hwy NW, P.O. Box 2204, Lilburn, GA 30047-1100, USA. Ph.: 872 216Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.