Recalls distributed in Ohio
These notices name Ohio 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.
5,400 stored notices name Ohio, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Ohio too — those are in the archive.
Reported Aug 1, 2018
Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medela Inc.
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
ARTIS Pheno, Fluoroscopic X-Ray system, Model Number 10849000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device 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
PROLENE SUTURE MONO BLUE - BV1755 Taper Point 3/8C, D10031
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
18 more products in this recall
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
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
VPS Rhythm ECG Accessory Pack with Johans Adapter, REF RHY-100-ECGJ Product Usage: To provide real time tip location…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
3 more products in this recall
FDA (openFDA device 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 18, 2018
Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in quilon parchment paper with a sticker label. Net wt. 2.5 oz,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nectar Foods LLC
FDA (openFDA food enforcement)
Reported Jul 18, 2018
Reliance 1227 Cart and Utensil Washer/Disinfector, FW03101, FW03102, FW03S003 Product Usage: The Reliance 1227 Cart and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jul 18, 2018
Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water, packaged in a PET bottles with a plastic cap, Net Wt.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talking Rain Beverage Co. Inc.
FDA (openFDA food 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
WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods Service, Inc.
25 more products in this recall
FDA (openFDA food 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
St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical Inc.
1 more product 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.