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.
Reported Sep 28, 2022
Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Sep 21, 2022
iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is used to move sample and wash solution from the aspiration…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcor Scientific, Inc.
FDA (openFDA device enforcement)
Reported Sep 21, 2022
MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 21, 2022
Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Heinz Foods Company
FDA (openFDA food enforcement)
Reported Sep 21, 2022
Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Sep 21, 2022
QIAcube Connect MDx, Model No. 9003070
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Sep 21, 2022
ZAP-X Radiosurgery System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zap Surgical Systems
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Sep 7, 2022
Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Epicurean Butter Co.
FDA (openFDA food enforcement)
Reported Sep 7, 2022
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Optikgeraete GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Abbott Jevity Complete, Balanced Nutrition with Fiber Ready to Hang enteral feeding container 1.5 Cal (for tube…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA food enforcement)
Reported Aug 31, 2022
NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bob's Red Mill Natural Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 31, 2022
(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 31, 2022
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materialise USA LLC
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2022
SteriSpine PS kit of 2 Multi-Axial Fenestrated Screws, model numbers/REF numbers KITM640, KITM645, and KITM740.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safe Orthopaedics LLC
FDA (openFDA device enforcement)
Reported Aug 31, 2022
NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Synapse Biomedical Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2022
Pizza John’s Recalls Pepperoni Pizza Products Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pizza John’s
USDA FSIS
Reported Aug 24, 2022
Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Albertsons Companies LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2022
BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Aug 17, 2022
cobas e801 Immunoassay Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Xhibit Telemetry Receiver, Model: 96280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
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.