Recalls distributed in Iowa
These notices name Iowa 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.
2,845 stored notices name Iowa, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Iowa too — those are in the archive.
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
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
Formula 418 Renal Balloon-Expandable Stent, RPN FOR418-18-80-6-12, Order Number (GPN) G56611 Balloon-expandable stent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
Dole "Classic Kit Light Cesar" fresh salad mix. Salad and topping Net Wt.7.7 OZ (218g), Dressing Net 2.2 FL OZ (65ml),…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dole Fresh Vegetables Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 20, 2020
Memantine Hydrochloride Extended-Release Capsules, 28 mg, 100 capsules per unit dose cartons, Rx only, Manufactured by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group
FDA (openFDA drug 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
da Vinci Xi Surgical System, IS4000 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three main…
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 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
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
Philips Brilliance iCT Computed Tomography X-Ray System; Model # 728306; UDI #s (01)00884838059474(21)100783,…
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
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
Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test; Material Number 425-2260; Lot number 18200A - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Labs
FDA (openFDA device enforcement)
Reported May 6, 2020
Elekta MONACO RTP Sytem, radiation treatment planning software system - Product Usage: The Monaco system is used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Inc.
1 more product in this recall
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
5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ocean Spray Cranberries Inc.
FDA (openFDA food 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 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
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)
Reported Apr 22, 2020
Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin for Gases and Electrolytes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2020
ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2020
"HEMOGLOBIN A1c CALIBRATORS *** REF 4P52-01 *** 307261/R03 *** S4P5X0 *** FOR USE WITH ARCHITECT" - Product Usage: use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Apr 15, 2020
LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter 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.