Recalls distributed in Maryland
These notices name Maryland in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,061 stored notices name Maryland, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Maryland too — those are in the archive.
Reported Feb 3, 2021
PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nihon Kohden America Inc.
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Blueberry Blizzard Coffee Cake, Item 259, Net Wt. 24 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nueske Applewood Smoked Meat, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 3, 2021
SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OMNIlife science Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respironics California, LLC
32 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 3, 2021
Samyang Buldak Extremely Spicy Hot Chicken Flavor Sauce Hot Chili Sauce Net Wt. 200 g (7.05 oz) Product of Korea UPC: 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Samyang Foods Co. Ltd.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 3, 2021
Weis Quality Cookies and Cream Ice Cream (48oz). Packaged in a squround paper container with a UPC of 041497-01253.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Weis Markets, Inc., Ice Cream Division
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 27, 2021
ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on the Access Family of Immunoassay Systems…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Penumbra Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2021
FITNESS LABS***Organic***Coconut Oil***Extra Virgin***16 fl. oz. (473 mL)***Carefully Designed and Distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Piping Rock Health Products
FDA (openFDA food enforcement)
Reported Jan 27, 2021
uPath software 1.1 and uPath software 1.1 IVD-INSW, Material numbers 08991871001 and 09077332001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2021
Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
AnshLabs - SARS-CoV2 IgM ELISA (u-Capture), IVD, REF: AL-1002, kit contents, Ab PLATE 1 X ! Plate, IgM Sample DIL 1 x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansh Labs, LLC
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 20, 2021
icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the monitoring of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
visby medical COVID-19 Test kit *** An in vitro diagnostic for the qualitative detection of SARS-CoV-2 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Visby Medical Inc.
FDA (openFDA device enforcement)
Reported Jan 13, 2021
Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported Jan 13, 2021
enGen Laboratory Automation System, enGen Track System, Catalog Number ENGEN - Product Usage: intended for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 6, 2021
Product Code: K05T-02533, Custom Inflation Kit, Custom K05 Sterile EO, Rx Only, (01)00884450255803 For…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 6, 2021
REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask with 8' Tubing, Rx Only, CE0482, (01)00709078003172 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Westmed, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 2, 2021
Courage Production, LLC. Recalls Ready-to-Eat, Fully Cooked Polish Sausage Products due to Misbranding and an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Courage Production, LLC.
USDA FSIS
Reported Dec 30, 2020
APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.