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 Aug 1, 2018
PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biscomerica, Inc.
FDA (openFDA food enforcement)
Reported Aug 1, 2018
Brivo XR385, model 5215463, Digital Diagnostic Radiographic System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers A1048503 and A1022103. Tissue and cell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies, Corp.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Nobel Biocare 17¿ Multi-Unit Abutment, Conical Connection NP, 2.5mm, REF 36614. Product Usage: Intended to be used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nobel Biocare USA LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Consumer Packaging: WELLSLEY FARM WILD CAUGHT MAHI-MAHI LOINS, UPC: 8 88670 00983 3, plastic 2lb retail bag, Keep…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Orca Bay Foods LLC
FDA (openFDA food enforcement)
Reported Aug 1, 2018
BLAST Bandage, sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tactical Medical Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
FDA (openFDA device enforcement)
Reported Jul 25, 2018
VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet SAS
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part Number 9735559, Visualase¿ Cooled Laser Applicator…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
UNI-CP, Model Numbers: 330021S, 330023S, 330025S, 330030S, 330025S, 30030S, 330217S, 330220S, 330225S, 330230S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NewDeal SA
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Ingenuity Digital PET/CT System, Model 882446 with the following UDI's: (01)00884838059559(21)900004…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jul 25, 2018
t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM Software version: 4.3.4.3, Firmware version: 004722, Firmware, Fuel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coca-Cola Company
FDA (openFDA food enforcement)
Reported Jul 18, 2018
BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 18, 2018
PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Safety Sideport Knife 1.0mm 45¿, REF 378210 Product Usage: Indicated to make stab incisions during ophthalmic surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec
FDA (openFDA device enforcement)
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Icelandic Provisions Inc.
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.