Recalls distributed in Michigan
These notices name Michigan 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.
4,580 stored notices name Michigan, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Michigan too — those are in the archive.
Reported Jun 10, 2020
safeCLINITUBES Blood Sampler;REF 942-892;D957P-70-100x1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnosis and treatment of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Absorb Health Advanced Joint Relief Joint Health; 510mg; 90 CAPSULES; Manufactured for: Absorb Health, 106 Countryside…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Absorb Health LLC
FDA (openFDA food enforcement)
Reported Jun 3, 2020
Epix latis GRASPER, 5 mm x 35 cm, REF C4130, Qty: 10, Sterile R, CE, Rx ONLY, UDI: (01)00607915110147
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
ISE Electrolyte Reference (2 X 2L) Reagent, REF A28937, UDI: 15099590202491 - Product Usage: are intended for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
CooperSurgical Dilator/Sound Set, Rx only, Sterile/EO, Made in South Korea, P/N MX21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Giraffe Shuttle. Upgrade Kits with part number 2109672-001 and 2109673-001 GTIN: 00840682110808.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Medtronic Confida Expandable Sheath, REF CES122230. To provide a guide for catheters or devices introduced into the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular Galway dba Medtronic Ireland
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Body Weight Support (BWS) Light; Model No. RB011; a component of C-Mill, Grail, M-Gait - Product Usage: is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Motek Medical B.v.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
GENTLEWAVE REF: FG-002-0001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonendo Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
Optilite Optilite Rheumatoid Factor Kit, Ref: LK151.OPT.A, IVD, Rx Only, UDI: 05051700020015 (kit ea. containing four…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported May 27, 2020
STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2020
Frames Direct Prescription Spectacle Lenses included in the frame brands
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Frames Direct
FDA (openFDA device enforcement)
Reported May 27, 2020
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Left, Sterile, Catalog # 504-02-54C-L, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
15 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2020
K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.K2M, Inc.
23 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3FR 6cm. REF/UDI 72627/ 00859821006674 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Access Scientific LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported May 20, 2020
Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US); 641417/641417-1157-1-01 (OUS); 641399/641399-4012-1-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported May 20, 2020
SureStep Foley Tray System - Product Usage: Intended for use in the drainage and/or collection and/or measurement of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
CuattroDR System Software, REF: SWR-00069-MD, UDI: B269SWR00069MD0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cuattro LLC
FDA (openFDA device enforcement)
Reported May 20, 2020
Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
Inpeco FlexLab, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: FLX-208-00, FLX-208-10 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
da Vinci Xi Surgical System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 20, 2020
Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Karl Storz Endoscopy
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.