Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,351–11,400 of 15,364
- 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
Food Recall · June 26, 2024
NANJING NUTRABUILDING BIO TECH C
Bovine Collagen Peptide. Powder, Grade A, Cowhide Source. Net Weight: 20.0 kg. Made in China.Potential Salmonella contamination.
- Class II
Medical Device Recall · June 26, 2024
FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD
DVOT SARS-CoV-2 ANTIGEN TEST KIT, Model Number FCY-AGT-01The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.
- Class II
Medical Device Recall · June 26, 2024
ENT RES 100 ML Non-Sterile W CLAMP, TUBING FLAG, & FEMALE LUER, Product Code 68-2230-28Certain 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
smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis infusion pumpsThe adapter input plug can become damaged or broken. If the input plug is damaged, the metal contacts to the body of the AC adapter may be exposed or one or more of the AC mains prongs may separate from the input plug.
- Class II
Medical Device Recall · June 26, 2024
Becton Dickinson Infusion Therapy Systems, Inc.
BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte Autoguard BC Shielded IV Catheter is intended to be iCatheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.
- Unclassified
Consumer Product Recall · June 25, 2024
MGA Entertainment, of Chatsworth, California
Miniverse Make It Mini Sets with Liquid ResinsThe recalled Make It Mini sets contain resins that, when liquid, can cause skin, eye, and respiratory irritation or sensitization when inhaled, touched, or ingested by children or adults. The resins contain acrylates (hydroxyethylmethacrylate "HEMA" and isobornyl acrylate "IBOA") in amounts prohibited in children's products by the Federal Hazardous Substances Act. After the resins cure, they no longer present this hazard.
- Class III
Drug Recall · June 25, 2024
Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC code: 8-40078-56497-0Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Class III
Drug Recall · June 25, 2024
Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Class III
Drug Recall · June 25, 2024
Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Class I
Drug Recall · June 25, 2024
Amerisource Health Services LLC
Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, a).100-count bottle ( NDC 68001-396-00), b) 500-count bottle (NDC 68001-396-03), Rx Only, Manufactured by: Glenmark PharmaceuticalFailed Dissolution Specifications
- Class II
Medical Device Recall · June 25, 2024
Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703 Straumann Tissue-Level-compatible WN Digital Analog, REF 9001303 3i Certain-compatiblDue to a manufacturing issue, the product has a out of specification rotation of the digital analog used to visually inspect dental abutments and restorations.
- Class II
Medical Device Recall · June 25, 2024
1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. TechThe tube may fall into the surgical site during the grasping process.
- Class III
Drug Recall · June 25, 2024
Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, NDC 73423-003-01; UPC Code: 8-40078-56493-2Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
- Class III
Food Recall · June 25, 2024
Sands Impex Inc. Dba Asli Fine Foods
Asli Sesame Seeds Brown 14oz., UPC: 7 03440 18270 0; 20 units per wholesale case.Product sample exceeded tolerance for pesticide Fenvalerate
- Class II
Medical Device Recall · June 25, 2024
HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant Kits or distributed separately: HeartMate 3 LVAS Implant Kit, US, Model: 1065Left ventricular assist system controller UI membrane/screen may lift along the edge of the controller housing, and if controller is exposed to fluid, ingress may occur, which may damage printed circuit board assemblies, which could result in unexpected and false positive alarms, loss of visual alarms, loss of user interface(use of buttons, loss of visual alarms,etc.), loss of power, and pump stop
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P, REF: 169-99 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class I
Food Recall · June 24, 2024
7-Eleven Simply Chicken Salad Sandwich, Keep Refrigerated, Flexible Packaging, 6.6oz (187g)Undeclared milk
- Class II
Food Recall · June 24, 2024
Orzo (vegan) Dried, net wt. 10oz in clear package with green/back printings on white label. UPC 810135110747.Product is recalled due to potential mold growth contamination.
- Class III
Drug Recall · June 24, 2024
Diflorasone Diacetate Ointment, USP, 0.05%, 60g tube, Rx only, Mfd. By: Lyne Laboratories, Inc., Brockton, MA 02301; Mfd. For: Rising Pharmaceuticals, Inc., East Brunswick, NJ 08816 NDC 64980-124-60Failed Impurities/Degradation Specifications: The impurity results at 12 months stability testing,did not conform to the specification limit.
- Class II
Food Recall · June 24, 2024
Campanelle (vegan) Dried, net wt. 10oz. in clear package with green/back printings on whie label. UPC 850049624022.Product is recalled due to potential mold growth contamination.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P, REF: 169-93 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P, REF: 169-92 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class I
Medical Device Recall · June 24, 2024
Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT 560 VENTILATOR/4096600, PURITAN BENNETT PB560 VENTILATOR EU-DIV/4096600-01, PURITAN BENNETT 560 VENTILATOR JAPAN/4096600-02Any single affected ventilator should only be used for the 10- year labelled service life, but if longer ventilatory support is required using more than one ventilator over time, the use of these devices for more than 14 years of cumulative duration may pose harm to health due to a volatile organic compound (VOC), 2-propanol, 1,3-dichloro released from some components in the ventilator gas pathway
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P, REF: 169-94 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P, REF: 169-90 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-14HH-P, REF: 169-86 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class I
Medical Device Recall · June 24, 2024
NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM Vital System versions: v1.0.0, v1.1.1, v1.3.2, v1.4.3. NIM Vital Nerve Integrity Monitor with below product descriptionPotential for false negative response on the NIM Vital Nerve Monitoring System
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P, REF: 169-97 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK MINI CR-4HH-P, REF: 169-115 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Drug Recall · June 24, 2024
Amerisource Health Services LLC
buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 60687-782Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow, REF: 169-131 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P, REF: 169-91 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Food Recall · June 24, 2024
Bakeshop Chocolate Chip Muffin 4 count, in clear plastic clamshell, UPC 4099100048278. 5 retail units per case.Undeclared Walnut
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-2HH-6FH, REF: 169-88 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK MINI CR-2HH-1FH-P, REF: 169-114 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-12HH-1FH, REF: 169-84 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class I
Food Recall · June 24, 2024
7-Eleven Simply Egg Salad Sandwich, Keep Refrigerated, Flexible Packaging, 6.8oz (193g)Undeclared milk
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P, REF: 169-98 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P, REF: 169-85 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P, REF: 169-96 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P, REF: 169-83 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 24, 2024
BD PYXIS MEDBANK TWR MN CR-2HH-6FM, REF: 169-89 containing software version 3.9.1.9Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
- Class II
Medical Device Recall · June 21, 2024
Olympus Corporation of the Americas
ESG-410 Electrosurgical Generator- In conjunction with electrosurgical accessories intended for cutting and coagulation of tissue in open, laparoscopic , and endoscopic surgeries Model/Catalog NumberElectrosurgical Generators ESG-410 does not power on upon use, may result in delays in initiating treatment or prolonged surgery
- Class I
Food Recall · June 21, 2024
Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged in 8.1oz vacuum foil, packaged within cardboard envelope. Keep Refrigerated at 38F or below.Potential contamination with Listeria monocytogenes
- Class II
Food Recall · June 21, 2024
Starter Bakery Multigrain Sourdough Bread with UPC 8 50025 60902 9Allergen (sesame seeds) declared in the ingredient statement but missing from the "Contains" statement
- Class II
Drug Recall · June 21, 2024
Zydus Pharmaceuticals (USA) Inc
Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg, packaged in a) 90-count bottles (NDC 68382-034-16) and b)1000-count bottles (NDC 68382-034-10), Rx only, Mfg. by: Zydus Lifesciences LtFailed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
- Class I
Drug Recall · June 21, 2024
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.