State

Michigan product recalls

72,969 recalls have nationwide distribution and so reach Michigan. 9,518 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total: 9,518
Critical: 1,556
Severe: 2,145
Most recent: 2026-09-16

Of the 9,518 recalls naming Michigan we have scored against our rubric, 1,556 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,145 (23%) are Severe.

Which agencies issued them

These figures cover only the 9,518 recalls whose distribution notice names Michigan specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4876–4900 of 82487

CriticalFDA (Food)·H-0150-2026·2025-10-29
Breakfast burritos and wraps recalled after egg ingredient tested positive for Listeria
M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.
Product
Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0154-2026·2025-10-29
IV burette sets recalled over missing internal shutoff valve component
ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.
Product
IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm) 150 ml Burette Set (Clave, Shut-Off) w/3-Way Stopcock, Clave, Graduated Adapter,
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0094-2026·2025-10-29
Basil pesto bowtie salad recalled over recalled pasta ingredient and Listeria
Kroger is recalling 5,567.4 lbs of Basil Pesto Bowtie Pasta Salad because the store-made deli item contains a pasta ingredient recalled for potential Listeria monocytogenes.
Product
Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fr
Category
Food
Distribution
28 states
CriticalFDA (Food)·H-0132-2026·2025-10-29
Shrimp scampi meals recalled over linguine linked to Listeria outbreak
Demers Food Group is recalling 12,962 cases of Scott & Jon's Shrimp Scampi with Linguine because it contains linguine recalled for Listeria monocytogenes and implicated in an ongoing outbreak.
Product
Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0084-2026·2025-10-29
Dried apricots recalled because the product contains undeclared sulfites
Turkana Food is recalling 352 cases of Floria Dried Apricots because the product contains undeclared sulfites.
Product
Floria Dried Apricots, 200 Gram packages, 40 packages per case .
Category
Food
Distribution
19 states
CriticalFDA (Devices)·Z-0136-2026·2025-10-29
Impella controllers recalled over purge pressure issues from retainer failures
Abiomed is recalling Automated Impella Controllers over the potential for purge pressure issues caused by purge retainer failures, covering 9,177 distributed units.
Product
Automated Impella Controller (AIC) labeled as the following with corresponding Product Codes: 1. AIC w/Impella Connect for ECP, Product Code: 1000432. 2. Dbl optical, AIC Impella Connect, Phg US, Product Code: 1000201. 3. Impella Controller, Packaged, AU, Product Code: 0042-00
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0070-2026·2025-10-29
Hemodialysis bloodline sets recalled over micro air bubbles from damaged connectors
B. Braun is recalling Streamline Bloodline Sets for Dialog because damaged arterial and venous patient connectors may cause micro-air bubbles in the bloodline and air-in-line alarms.
Product
Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG Model/Catalog Number: SL-2010M2096 Software Version: N/A Product Description: STREAMLINE BLOODLINE SET FOR DIALOG Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V737000·2025-10-29
Mazda CX-50 front suspension bolts may allow wheel detachment
Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.
Product
MAZDA — MAZDA CX-50, CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0109-2026·2025-10-29
Frozen organic spinach recalled over potential Listeria monocytogenes contamination
Sno Pac Foods is recalling 4,006 cases of Frozen Organic Spinach in 10 oz poly bags because the spinach has the potential to be contaminated with Listeria monocytogenes.
Product
Frozen Organic Spinach Net Wt. 10 oz (283.5g) poly bags packaged under the following brands: 1. Sno Pac Frozen Vegetables, UPC 0 24284-96910 5. Keep Frozen. Packed and Distributed by: Sno Pac Foods, Inc., 521 West Enterprise, Caladonia, MN 55921. 2. ***This product di
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-0239-2026·2025-10-29
Automated microbiology systems recalled after service credentials were accessed by unauthorized actor
Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0238-2026·2025-10-29
BD MAX instruments recalled after service credentials accessed by unauthorized actor
Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.
Product
BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0215-2026·2025-10-29
Clinical analyzer modules recalled over dilution factor software anomaly affecting results
Beckman Coulter is recalling 160 DxC 500i Clinical Analyzer modules over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxC 500i Clinical Analyzer Modules, DxC 500 AU Module w/ISE, DxC 500i (Part Number C63522), DxC 500 AU Module, DxC 500i (Part Number C63521), and Access 2 Module, DxC 500i (Part Number C13252)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0234-2026·2025-10-29
Prefilled saline flush syringes recalled over sodium chloride concentration shortfall
Medline is recalling 8,267,150 Excelsior Medical 0.9% Sodium Chloride prefilled flush syringes because a limited quantity may not meet the required concentration of sodium chloride.
Product
Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush syringes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0211-2026·2025-10-29
Gastroduodenal sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of Salem Sump PVC gastroduodenal tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0288-2026·2025-10-29
Defibrillator pad packs recalled over damaged pins disrupting electrical contact
HeartSine Technologies is recalling 1,291,165 Pad-Pak units because defibrillator pads may contain damaged pins that disrupt the mechanical fit and electrical contact.
Product
HeartSine Pad-Pak, REF: PAD-PAK-01, PAD-PAK-02, PAD-PAK-03, PAD-PAK-04, PAD-PAK-07, PAD-PAK-03J, PAD-PAK-04J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0096-2026·2025-10-29
Ready rice pouches recalled over possible presence of stones in product
Mars Foods US is recalling 1,075 cases of Ben's Original Ready Rice Long Grain & Wild because of the possible presence of stones in the product.
Product
Ben's Original Ready Rice Long Grain & Wild, 8.8oz., UPC 0 54800 42331 6. 12 retail units per wholesale case
Category
Food
Distribution
9 states
HighFDA (Food)·H-0114-2026·2025-10-29
Frozen cooked salad shrimp recalled over possible cesium 137 contamination
Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.
Product
Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-0227-2026·2025-10-29
Bipolar hip heads recalled downstream after femoral components failed transit testing
Theken Companies is recalling 409 iNSitu Bipolar Hip System head assemblies in a downstream recall after BioPro femoral components failed transit testing, risking sterile barrier issues.
Product
iNSitu Bipolar Hip System, Bipolar head implant Part ID Description 10-22-0038 Bipolar Head Assembly, Size 38mm 10-22-0040 Bipolar Head Assembly, Size 40mm 10-22-0042 Bipolar Head Assembly, Size 42mm 10-22-0044 Bipolar Head Assembly, Size 44mm 10-22-0046 Bipolar Head Asse
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0035-2026·2025-10-29
Alcohol prep pads recalled from one lot as a subpotent drug
Medline is recalling 222,800 alcohol prep pads from one lot because the product is subpotent.
Product
Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0233-2026·2025-10-29
Oral thermometer probes recalled after being programmed with rectal configuration
Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.
Product
Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0098-2026·2025-10-29
Whole grain brown ready rice recalled over possible stones in product
Mars Foods US is recalling 315 cases of Ben's Original Ready Rice Whole Grain Brown because of the possible presence of stones in the product.
Product
Ben's Original Ready Rice Whole Grain Brown, 8.8oz., UPC 0 54800 42334 7. 12 retail units per wholesale case.
Category
Food
Distribution
9 states
HighFDA (Food)·H-0112-2026·2025-10-29
Frozen cooked shrimp recalled across four brands over cesium 137 contamination
Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.
Product
Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-0216-2026·2025-10-29
Immunoassay analyzers recalled over dilution factor anomaly affecting patient results
Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.
Product
DxI 9000 Access Immunoassay Analyzer, Part Number C11137
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0116-2026·2025-10-29
Frozen shrimp skewers recalled in expanded cesium 137 contamination action
Southwind Foods is recalling Great American branded frozen raw shrimp skewers made under insanitary conditions in which the product may have been contaminated with Cesium-137.
Product
Great American branded Frozen raw shrimp skewer; 1lb bag UPC: 829944002716; 829944002372
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-0206-2026·2025-10-29
ENFit sump tubes recalled after anti-reflux valve breakage complaints
Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.
Product
Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
Category
Medical Device
Distribution
Distributed nationwide