Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,501–3,550 of 15,186
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX600. Product Number: 865242.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/FiberTape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP30. Product Number: M8002A.Potential issue where the IntelliVue monitors did not alarm.
- Class I
Food Recall · October 31, 2025
Bulk and Organic Organic Moringa Powder, 44.1lbs bagPossible Salmonella Richmond
- Class II
Drug Recall · October 31, 2025
Wecare Enema, 4.5 Fl Oz/133mL, Manufactured for: Dynarex Corporation, 11 Dynarex Corporation, MIddletown, NY 10941 USA, Made in India, NDC 67777-402-01.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP2. Product Number: M8102A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NTape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX550. Product Number: 866066.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
darby dental supply, MEPIVACAINE, Mepivacaine HCI 3% (30mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, ManufacturDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
Benco dental Graham CHEMICAL CO., Mepivacaine HCI 3% (30 mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, DistributeDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Wecare Calasoothe, Net wt. 4 oz (113 g), Manufactured for: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, NDC 67777-234-04.cGMP deviations
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
3% Polocaine DENTAL, Mepivacaine Hydrochloride 3% (30mg/mL) (Mepivacaine HCI Injection, USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for DentsplyDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX450. Product Number: 866062.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
OraVerse, (Phentolamine Mesylate) Injection, 0.4 mg/1.7mL, packaged in a carton containing 10 cartridges, 0.4 mg/1.7mL, Rx only, Made in Canada by Novocol Pharmaceutical of Canada, Inc., Distributed bDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Nivagen, Zinc Oxide Ointment, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA Made in India, NDC 75834-170-01.cGMP deviations
- Class II
Drug Recall · October 31, 2025
Dynagel, Moisturizing Wound Hydrogel, Net Wt. 3oz (84.7 g), Manufactured for: Dynarex Corporation, 16 Glenshaw Street, Orangeburg, NY 10962, UPC 61784128016.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP60. Product Number: M8005A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Lanashield Skin Barrier, 4 oz. (113 g), Manfuactured for: Dynarex Corporation, 10 Gleshaw Street, Orangeburg, NY 10962 USA, Made in India, UPC 616784126319.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX800. Product Number: 865240.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
Olympus OER-ProInform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP70. Product Number: M8007A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
2% Xylocaine DENTAL with Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose cartridges, 1.7 mL each, Rx only, Manufactured for DentsplyDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX400. Product Number: 866060.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
Cook-Walte, Carbocaine 3% (30 mg/mL), (mepivacaine hydrochloride Injection, USP), packaged in a carton containing 50 Single-Dose Cartridges, 1.7 mL, Rx only, Manufactured by Novocol Pharmaceutical ofDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
Lidocaine HCI 2% and Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for Patterson DeDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Multi-Measurement Module X3. Product Number: 867030.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX850. Product Number: 866470.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX750. Product Number: 866471.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
WeCare, Zinc Oxide Ointment, Net Wt. 15 oz/425 g, Manuactured for: Dynarex Corporation, 11 Dynarex Drive, Middletown, NY 10941, Made in India, NDC 67777-223-05.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
Olympus OER-EliteInform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- Class II
Medical Device Recall · October 31, 2025
Olympus OER-MiniInform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- Class II
Food Recall · October 31, 2025
First & Last Tavern Marinara Sauce (tomato & basil) 26 FL OZ (1 lb, 10 oz) 737gMay be contaminated with Clostridium botulinum
- Class II
Food Recall · October 31, 2025
First & Last Tavern Puttanesca Sauce (olives, capers, hot peppers) 26 FL OZ (1 lb, 10 oz) 737gMay be contaminated with Clostridium botulinum
- Class II
Food Recall · October 31, 2025
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lidWheat and Soy missing allergens from the product Contains Statement.
- Class II
Drug Recall · October 31, 2025
Dynashield Skin Protectant, Net Wt. 16 oz (453.6 g), Manufactured for: Dyrnarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, USA, Made in India, NDC 67777-407-04.cGMP deviations
- Class II
Drug Recall · October 31, 2025
Dynashield, 4 oz cream (113 g), Manufactured for: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10852, USA, Made in India, NDC 67777-407-03.cGMP deviations
- Class II
Drug Recall · October 31, 2025
Phytonadione Injectable Emulsion, USP 10mg/mL, 10x1 mL Single-Dose Vial/carton, Rx Only, Mfd. by: Cipla Ltd. India At M/s Immacule Lifesciences PVT. Ltd. India. Mfd. for: Cipla USA, Inc. Warren, NJ 07Failed Stability Specifications: Observed OOS results: eg results for colour index
- Class II
Food Recall · October 31, 2025
INDIAN COOKWARE AND APPLIANCE LLC
ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIAPotential contamination due to leachable lead.
- Class II
Food Recall · October 31, 2025
First & Last Tavern Traditional Pasta Sauce (meat flavored) 26 FL OZ (1 lb., 10 oz) 737gMay be contaminated with Clostridium botulinum
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP90. Product Number: M8010A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX700. Product Number: 865241.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX500. Product Number: 866064.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BraTape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP50. Product Number: M8004A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP80. Product Number: M8008A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX100. Product Number: 867033.Potential issue where the IntelliVue monitors did not alarm.