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.
4,635 stored notices name Michigan, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Michigan too — those are in the archive.
Reported Apr 30, 2025
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ihb Operations B.v.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Apr 30, 2025
Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Request Foods Incorporated
3 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 30, 2025
Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.S Martinelli & Company
FDA (openFDA food enforcement)
Reported Apr 30, 2025
Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Supherb Farms
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 30, 2025
Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containers
High riskUsing this product could cause serious injury, illness or death — stop using it now.Walker's Fruit Basket and Press House
FDA (openFDA food enforcement)
Reported Apr 23, 2025
Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 198 Software Version: N/A Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Avanos Medical, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 23, 2025
BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 23, 2025
Farmer House Preserve Olive Strips
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lins Waha International Corp.
FDA (openFDA food enforcement)
Reported Apr 23, 2025
Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Apr 23, 2025
t:slim X2 Insulin Pump with Interoperable Technology
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 23, 2025
HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec LLC
FDA (openFDA device enforcement)
Reported Apr 23, 2025
BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tristar Food Wholesale Co. Inc.
FDA (openFDA food enforcement)
Reported Apr 16, 2025
BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 16, 2025
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Qapel Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2025
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Apr 9, 2025
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 9, 2025
Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Apr 5, 2025
Johnsonville, LLC, Recalls Cheddar Bratwurst Product Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Momence Real Estate
USDA FSIS
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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.