All Recalls

1335 recalls found

Date▼	Source	Product	Brand▼	Severity	Units▼
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. OSC COLE	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260.	Philips North America	Class II	N/A
2026-05-06	FDA Device	FDA Recall: i-STAT EG7+ cartridge; List Number: 03P76-25;	Abbott Point Of Care Inc.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Numbe	Advanced Bionics, LLC	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF,	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. PLASTICS	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Drug	FDA Recall: GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laboratories, Inc	Alcon Research LLC	Class II	N/A
2026-05-06	FDA Food	FDA Recall: Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Produ	HEMU TRADING INC	Class I	N/A
2026-05-06	FDA Device	FDA Recall: epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN):	Siemens Healthcare Diagnostics Inc	Class II	N/A
2026-05-06	FDA Drug	FDA Recall: Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr.	Hikma Pharmaceuticals USA INC	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. SPINE PROCE	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Drug	FDA Recall: iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Distributed	Thea Pharma, Inc.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor batt	WHILL, INC.	Class I	N/A
2026-05-06	FDA Device	FDA Recall: WHILL Model F, with software versions before HMI: 2.23 / MC: 1.05; the device is an indoor/outdoor,	WHILL, INC.	Class I	N/A
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPNG NEURO 1X1	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Brand Name: Leksell Vantage Arc System REF: 1053958	Elekta, Inc.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges (4077 in total), LAMINECTOMY, CRANI	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Device	FDA Recall: VACUUM BAG SU LARGE, Non-sterile specimen container, Model/Catalog Number: 68409SS	Milestone S.R.L.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroes	Medline Industries, LP	Class II	N/A
2026-05-06	FDA Device	FDA Recall: BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use	Becton Dickinson & Co.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MICRODIS	Medline Industries, LP	Class II	N/A
2026-05-06	NHTSA	Contact with Drive Belt Pully May Damage and Cause Oil Lines to Leak	Corp. Micro Bird, Inc.	N/A	902
2026-05-06	FDA Food	FDA Recall: Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM)	LACTALIS CANADA, INC	Class II	N/A
2026-05-06	FDA Food	FDA Recall: KLG, Kesar Mukhwas, perishable, 24 months, flexible plastic, 200 gm, 818812022208, Ganesha Enterpris	Ganesha Enterprises LLC	Class II	N/A
2026-05-06	FDA Drug	FDA Recall: fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg p	Wells Pharma of Houston LLC	Class II	N/A

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