Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,101–7,150 of 15,271
- Class I
Medical Device Recall · April 17, 2025
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate)REF: 0092300Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
- Class I
Medical Device Recall · April 17, 2025
Bard Blakemore Esophageal-Nasogastric Tube (Adult) REF: 0092100Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
- Class II
Food Recall · April 17, 2025
Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages; Ingredients Soybean, Flour, Salt, Water, Potassium Sorbate; UPC: 6917799000385Product contains undeclared wheat.
- Class I
Medical Device Recall · April 17, 2025
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8" (20.3cm) Balloon X-Ray Opaque RubberDue to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
- Class II
Food Recall · April 17, 2025
Mild Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54632. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class II
Medical Device Recall · April 17, 2025
WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.Incorrect blister labelling.
- Class I
Medical Device Recall · April 17, 2025
Bard¿ Single Intragastric Linton Balloon Tube, REF: 0092740Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
- Class II
Food Recall · April 17, 2025
Pineapple Mango Salsa is refrigerated product, packaged in Polypropylene container, net wt. 13 oz, UPC 1 18738 63010. San Juan Salsa Co. WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Unclassified
Consumer Product Recall · April 17, 2025
YiWuShiJingYuDianZiShangWuYouXianGongSi, dba Eonroacoo, of China
COMEONROA Infant SwingsThe swings pose a suffocation risk because they were marketed for infant sleep, and they have an incline angle greater than 10 degrees, in violation of the Safe Sleep for Babies Act. In addition, the swings fail to meet mandatory warning requirements under the swing standard and are missing the required warnings and instructions for consumer products containing button cell and coin batteries under Reese's Law.
- Unclassified
Consumer Product Recall · April 17, 2025
Shanghai Chushuo Electronic Commerce Co. Ltd., of China
Joydeco Roller Window ShadesThe recalled roller shades have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window coverings are in violation of the federal regulations for window coverings and present a substantial product hazard. The shades also violate labeling requirements for window coverings.
- Unclassified
Consumer Product Recall · April 17, 2025
American Bolt and Screw, of Ontario, California
Tip-Over Restraint KitsThe plastic zip tie used with the recalled furniture tip kits can become brittle or break, which can allow a clothing storage unit that is anchored to the wall to detach during a furniture tip-over event, posing a tip-over and entrapment hazard that can result in death or serious injuries to children.
- Class II
Food Recall · April 17, 2025
Hot Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54634. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class II
Food Recall · April 17, 2025
Medium Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54633. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class I
Medical Device Recall · April 17, 2025
Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) REF: 0092110Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.
- Unclassified
Consumer Product Recall · April 17, 2025
Casely Inc., of Brookyln, New York
Casely Wireless Portable Power BanksThe lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.
- Unclassified
Consumer Product Recall · April 17, 2025
Liangyu Technology Co., Ltd., dba Leetous, of China
Glow Sticks and Glasses Party Pack ToysThe glow sticks and glasses violate the mandatory federal battery-operated toy regulation because the button cell batteries are in a compartment that can be opened easily without requiring the use of a common household tool. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns or death, posing an ingestion hazard to children.
- Unclassified
Consumer Product Recall · April 17, 2025
The North Face, a division of VF Outdoor LLC, of Denver, Colorado
The North Face Women's Shellista V Mid Waterproof BootsThe hook of one boot can catch on the lace of the other boot, posing a fall hazard to the consumer.
- Class II
Medical Device Recall · April 16, 2025
VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic testIt was determined that the consumable issue may result in No Call - INT CTL 1 and/or False Negative results on a small portion of the lot of test cartridges.
- Class II
Medical Device Recall · April 16, 2025
Remote Diagnostic Technologies Ltd.
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer)software issue that causes an error screen on a portable vital signs monitor when attaching video Laryngoscope.
- Class I
Food Recall · April 16, 2025
Enoki Mushroom in a 200g, green plastic package marked with UPC Barcode 6975730520101 on the back label and labeled as distributed by Hofood99 Inc., 21903 56th Ave Oakland Gardens, NY 11364Product is contaminated with Listeria monocytogenes.
- Class II
Food Recall · April 16, 2025
Advance Food International Inc.
National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.: 1 Kg (35.27 oz)/ 2.20lb; Ingredients: Kasundi (Peeled Mango), Canola Oil, Cabbage, Salt, Mixed Spices, Vinegar, Sodium Benzoate as preservatProduct contains elevated levels of lead (0.0649 mg/kg)
- Class II
Drug Recall · April 15, 2025
Urodel, Urinary Tract Infection Symptoms Relief, Homeopathic, 30 chewable tablets per bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-406-30cGMP deviations
- Class II
Drug Recall · April 15, 2025
FentaNYL 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (0.1%) added to 250 mL, 0.9% Sodium Chloride Injection (For Epidural Use Only), Sterile, Single-Use Container, Rx Only, Apollocare, 3801 Mojave Ct,Lack of Assurance of Sterility
- Class II
Drug Recall · April 15, 2025
DoloDent Maximum Strength Toothache Drops, Homeopathic Oral Drops, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-400-15cGMP deviations
- Class I
Food Recall · April 15, 2025
Bone & Joint Restore. 180 capsules in a plastic bottle. Shelf life two years. Store at ambient temperature. Optimal Carnivore LLC 1603 Capitol Ave Ste 310 WY371 Cheyenne, WY 82001Potential for contamination with salmonella.
- Class II
Drug Recall · April 15, 2025
Dexonto 0.4% (dexamethasone sodium phosphate) solution 20 mg/5 mL (4 mg/mL), Rx Only, 12 - 5 mL Single Dose Units per box, Preservative Free, For Iontophoresis Use Only, Non-Sterile Product, Not for ILabeling: Incorrect or Missing Lot and/or Expiration date: Individual vials of Dexonto 0.4%, are labeled correctly with the BUD of 12/25/2024, however, the outer box on some of the Dexonto 0.4% are labeled incorrectly with a BUD of 12/25/2025.
- Class II
Drug Recall · April 15, 2025
Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02cGMP deviations
- Class III
Drug Recall · April 15, 2025
HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01.Superpotent Drug: Assay/potency result for hydromorphone HCl in the compounded stability lot was higher than specification..
- Class II
Drug Recall · April 15, 2025
DoloEar Earache Drops, Homeopathic, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-401-15cGMP deviations
- Class II
Medical Device Recall · April 15, 2025
Remote Diagnostic Technologies Ltd.
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007Patient Monitor software update to address issues:1)May freeze at startup with MPM Application error and Attention Restart Required messages,2)Monitor may freeze and reboot at start of 12-lead ECG or after, 3)May reboot after intermittent connection with Smart Mount, 4) 12-lead ECG measurements with Louvain algorithm and software before vx.36 could produce inaccurate rhythm/morphology statements.
- Class II
Drug Recall · April 15, 2025
Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99cGMP deviations
- Class II
Drug Recall · April 15, 2025
Kingskin, Elimina Las Verrugas, For the removal of common warts, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-409-15cGMP deviations
- Class II
Medical Device Recall · April 15, 2025
Siemens Healthcare Diagnostics, Inc.
Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY Calibrator do not meet the assay Instructions for Use (IFU) reference interval due to calibrator instability resulting in increased positive bias.
- Class II
Medical Device Recall · April 15, 2025
Siemens Healthcare Diagnostics, Inc.
ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376.Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY Calibrator do not meet the assay Instructions for Use (IFU) reference interval due to calibrator instability resulting in increased positive bias.
- Class II
Drug Recall · April 14, 2025
Breckenridge Pharmaceutical, Inc
Duloxetine Delayed-Release Capsules USP, 30 mg, a.) 90-count bottles (NDC# 51991-747-90), b.) 1000-count bottles (NDC 51991-747-10), Rx Only, Manufactured by Towa Pharmaceutical Europe, S.L. DistributCGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
- Class II
Medical Device Recall · April 14, 2025
Ortho-Clinical Diagnostics, Inc.
VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges, of 18 slides per cartridge, for a total of 90 slides.Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton, foil wrapper, and cartridge (cart) label.
- Class I
Drug Recall · April 14, 2025
ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
- Class II
Food Recall · April 14, 2025
La Victoria Cilantro Salsa; Med; Net Wt 15.5 OZ; UPC# 0 72101 34470 3; Distributed by: Megamex Foods, LLC Orange, CA 92868Firm's salsa product was potentially manufactured with a recalled ingredient (Fresh Cilantro containing foreign objects "wood pieces")
- Class II
Drug Recall · April 14, 2025
Breckenridge Pharmaceutical, Inc
Duloxetine Delayed-Release Capsules USP, 60 mg, 1000-count bottles, Rx Only, Manufactured by Towa Pharmaceutical Europe, S.L., Distributed by Breckenridge Pharmaceutical, Inc. Berkeley Heights, NJ 079CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
- Class I
Drug Recall · April 14, 2025
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
- Class I
Drug Recall · April 14, 2025
Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
- Class I
Drug Recall · April 14, 2025
MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
- Class II
Drug Recall · April 14, 2025
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
ChlorproMAZINE Hydrochloride Tablets, USP, 10 mg, packaged in cartons of 100 TABLETS (10x10), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7129-61CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
- Class II
Medical Device Recall · April 14, 2025
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screThe perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.
- Class I
Drug Recall · April 14, 2025
Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
- Class II
Medical Device Recall · April 14, 2025
Plus Initial Drill, Article Number: 103.170;The referred batch was produced without the laser engraving of 7 mm.
- Class II
Medical Device Recall · April 14, 2025
Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The Glidewell HT" Implant Twist Drill is indicated to prepare the site forDue to packaging mix up. Package of finished devices were reported to have an incorrect finished device package inside.
- Class II
Food Recall · April 13, 2025
MAGIC FLAME, HULLED SUNFLOWER KERNELS, BAKERY GRADE, 501b. Bag, Three ply Paper bags, 1100 Paper bags x 50 Ib. on 20 pallets. Store in dry warehouse, room temperatureGlass fragments found in finished product.
- Class II
Medical Device Recall · April 13, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN Patient Drape, 8mm Adapter Plug Kit REF AP8MMN UDI code: (01)10748426139Due to non-sterile products being labeled as sterile
- Class II
Food Recall · April 12, 2025
Multigrain Sourdough , 18 oz, Paper carton (corrugated), CP12, FrozenGlass fragment found on top of bread.