All recall categories

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.

4,005 stored notices name Maryland, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Maryland too — those are in the archive.

Medical devices

Reported Apr 20, 2022

IntraSight Mobile IVUS Systems, Model: 797415, Part numbers: 300002018101, 300002018102

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Volcano Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

BenchMark ULTRA and DISCOVERY ULTRA Instruments

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Volcano Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 6, 2022

Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties Net Wt, 42.3 (1.2 kg). 12 retail packages per…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cavendish Farms

FDA (openFDA food enforcement)

Medical devices

Reported Apr 6, 2022

FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Illumina NextSeq 550Dx, REF: 20005715, CE, IVD

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Illumina, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RaySearch America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 30, 2022

Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml 12 units per case . Tetra Pak paper carton.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Flow Beverages Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 30, 2022

Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Alinity s System software version2.8.0, REF LN 06P16-01, IVD, OEI: (01)00380740138479 The Alinity s System is intended…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

10 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 23, 2022

Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fdmr, Inc. dba Suji's Korean Cuisine

FDA (openFDA food enforcement)

Medical devices

Reported Mar 23, 2022

Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Mycoplasma genitalium Control Panel (Inactivated Pellet)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 23, 2022

Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456.…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

PS Seasoning & Spices, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 23, 2022

All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Royal Ice Cream Company Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2022

ExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brainlab AG

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2022

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2022

Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Factor

FDA (openFDA food 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.