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 May 20, 2020
Ra Medical Systems DABRA Catheter 5F (1.5mm), REF: 1222-5000-01, LOT: 18-090400-094, USE BY: 2019-09-24, MFR DATE:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ra Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496; REF/UDI: 257-1810D(01)10818788021493 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
REF: AH7117 111" 10 Drop Admin Set w/2 Inj Sites, Rotating Luer, Sterile R, For Veterinary Use Only, (01) 1 0887709…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Inpeco FlexLab Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
ICU Medical Cogent Hemodynamic Monitoring System, Cogent Item Number 58400-000, UDI: (01)00840619079499
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
Nexus Universal with OptiBond Universal, Universal Adhesive Resin Cement, Trial Kit, Ref # 36990 - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerr/Pentron, dba Kerr Corporation and Pentron Clinical
FDA (openFDA device enforcement)
Reported May 6, 2020
PreludeSYNC DISTAL Radial Compression Devices, SDRB-REG-LT, SDRB-REG-RT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079 Image guidance in diagnostic, interventional and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2020
Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
9 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2020
Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Apr 29, 2020
ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips, Model Number 110028522 - Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2020
Enoki Mushroom; 7.5oz (200g); UPC #831211204181; packed in clear plastic bag with green label; imported from Green Co.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.H & C Food Inc.
FDA (openFDA food enforcement)
Reported Apr 29, 2020
RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and Model RSPOl)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rayner Intraocular Lenses Limited
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Merlin PCS 3650 Software Upgrade Kit, REF 3330 St. Jude Medical The MerlinTM Patient Care System (MerlinTM PCS) Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Nitinol Thermocouple Electrode, 10 cm - Product Usage: The TCN Electrode is indicated for use in RF heat lesioning of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2020
Canon Aquilion Lightning, Model TSX-036A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
7 more products in this recall
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.