State

Michigan product recalls

73,576 recalls have nationwide distribution and so reach Michigan. 9,551 additional recalls listed Michigan specifically in their distribution scope.

What the numbers show

Total: 9,551
Critical: 1,566
Severe: 2,550
Most recent: 2026-10-24

Of the 9,551 recalls naming Michigan we have scored against our rubric, 1,566 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,550 (27%) are Severe.

Which agencies issued them

These figures cover only the 9,551 recalls whose distribution notice names Michigan specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

551–575 of 83127

SevereFDA (Food)·H-1367-2026·2026-09-23
Taylor Fresh Foods Recalls Pico De Gallo Due to Salmonella Risk
Taylor Fresh Foods Inc. is recalling 12-ounce Pico De Gallo distributed by WAWA due to potential Salmonella contamination.
Product
Pico De Gallo. Ingredients: Tomato, Red Onion, Green Bell Pepper, Tomato Juice (Tomato Juice from Concentrate [Water, Concentrated Juices from Tomatoes], Salt, Vitamin C [Ascorbic Acid]), Lime Juice, Garlic, Salt, Cilantro. Net Wt: 12 oz. Keep Refrigerated. Distributed By: WAWA…
Category
Food
Distribution
27 states
SevereFDA (Food)·H-1336-2026·2026-09-23
Foods Alive Organic Moringa Leaf Powder Recalled for Salmonella Risk
Foods Alive Inc. is recalling 1,691 pouches of organic moringa leaf powder due to potential Salmonella contamination. The product was sold nationwide in the US and UAE.
Product
Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·H-1351-2026·2026-09-23
Taylor Fresh Foods Recalls Spicy Guacamole Due to Salmonella Risk
Taylor Fresh Foods is recalling 13-ounce Spicy Guacamole products due to potential Salmonella contamination. The recall covers specific lots distributed in Tennessee and Texas.
Product
Spicy Guacamole. Ingredients: Guacamole, Pico De Gallo. Spec Sheet: Guacamole (Avocado, Pico De Gallo, Serrano Peper, Lime Juice, Salt, Pepper); Pico De Gallo (Cilantro, Jalapeno Pepper, Tomato, Yellow Onion) Net Wt: 13 oz. Keep Refrigerated. Distributed By: Taylor Farms Inc.…
Category
Food
Distribution
27 states
SevereFDA (Devices)·Z-3108-2026·2026-09-23
AVID Medical Recalls Halyard IV Start Kits Due to Mold Contamination
AVID Medical is recalling Halyard IV Start Kits because they contain applicators contaminated with Aspergillus penicillioides.
Product
Halyard IV START KIT NON-STERILE REF: KRIV26-02
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3130-2026·2026-09-23
Nova Biomedical StatStrip Glucose Meter Recalled for Data Error
Nova Biomedical is recalling StatStrip Glucose meters due to a software defect that may assign patient test results to the wrong medical record.
Product
StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3149-2026·2026-09-23
Abiomed Recalls Impella Optical Controllers Due to Purge Flag Component Failure
Abiomed is recalling 1,422 Impella Optical Controllers because a purge flag component may fail, causing purge cassette recognition issues.
Product
Impella Optical Controller with the below product descriptions and corresponding Product Codes. 1. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU. 2. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU. 3. Impella Optical Controller…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2984-2026·2026-09-23
Bard Access Systems Recalls Power-Trialysis Dialysis Catheters
Bard Access Systems is recalling Power-Trialysis dialysis catheters as a downstream action to a Class I recall.
Product
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605240; Power-Trialysis Short-Term Straight Dialysis Catheter, REF…
Category
Medical Device
Distribution
50 states
HighNHTSA·26V608000·2026-09-23
Forest River Recalls 2025-2026 Cedar Creek Trailers Due to Door Blockage
Forest River is recalling 2025-2026 Cedar Creek fifth wheel trailers because a sleeper sofa may block the bunkroom door, potentially delaying emergency exits.
Product
FOREST RIVER — FOREST RIVER CEDAR CREEK
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3207-2026·2026-09-23
Medline Anesthesia Pain Kits Recalled for Potential Sterility Compromise
Medline Industries is recalling 341 anesthesia pain kits due to open sterile seals that may compromise sterility and lead to patient infection.
Product
Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3200-2026·2026-09-23
Howmedica Recalls Orthopaedic Implants Due to Potential UHMWPE Oxidation
Howmedica is recalling specific orthopaedic implant components made with aged UHMWPE material that may oxidize, potentially leading to increased wear and device failure.
Product
DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-800 C-M062-7-500 C-M063-2-600 SELF-PRESSURIZING GLENOID SIZE 9 C-M063-5-000 SHOULDER - GLENOID #11 5361-6111 SHOULDER - GLENOID #5 5361-6105 SHOULDER…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3156-2026·2026-09-23
ICU Medical Recalls Plum Administration Sets Due to Drip Chamber Discoloration
ICU Medical is recalling Plum administration sets because drip chambers may contain black specks or discolored PVC material. The presence of particulate matter in the fluid path has not been ruled out.
Product
Plum administration sets
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3192-2026·2026-09-23
Datex-Ohmeda Et Control Software Recalled for Anesthetic Delivery Interruption
Datex-Ohmeda is recalling 410 Et Control software units for anesthesia gas machines that may interrupt anesthetic delivery, requiring clinician intervention to prevent decreased patient effect.
Product
Et Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents, Field replaceable unit (FRU) part numbers: 1011-8000-000-S, 5700665
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3146-2026·2026-09-23
Maquet Percutaneous Insertion Kit Recalled for Sterile Barrier Integrity Issues
Maquet is recalling Percutaneous Insertion Kits because the packaging may not consistently maintain sterile barrier integrity, posing a risk of infection.
Product
Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3208-2026·2026-09-23
Medline Recalls Minor Pack Convenience Kits Due to Open Sterile Seals
Medline Industries is recalling 459 units of Minor Pack convenience kits because open sterile seals may compromise sterility and lead to patient infection.
Product
Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3137-2026·2026-09-23
Medline Open Heart A Pack Kits Recalled for Sterility Concerns
Medline is recalling 135 Open Heart A Pack kits in California due to a potential sterile barrier breach in the RCSP cannulae, posing a risk of infection.
Product
Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3175-2026·2026-09-23
Happiest Baby SNOO Sleep Sack Recall for FDA Review Status
Happiest Baby, Inc is recalling 1,055 units of SNOO Sleep Sacks because Extra Small and Extra Large sizes have not been reviewed for safety and effectiveness by the FDA.
Product
Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101 S2107-110
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3198-2026·2026-09-23
Howmedica Recalls Triathlon Hinge Inserts Due to Material Aging
Howmedica is recalling Triathlon hinge inserts made with aged polyethylene that may wear excessively, potentially causing device fracture or the need for revision surgery.
Product
TRIATHLON HINGE INSERT SIZE 4 11MM 5612-P-411 TRIATHLON HINGE INSERT SIZE 4 13MM 5612-P-413 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3164-2026·2026-09-23
Nuclein DASH Rapid PCR Instrument Recalled for Software Issue
Nuclein LLC is recalling 182 DASH Rapid PCR Instruments due to a software issue. The recall affects units distributed in 18 US states.
Product
Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2, 6.0.4, 6.0.5, 6.0.6 Product Description: The DASH¿ Rapid PCR Instrument (DASH Instrument) is an automated, fluorescence-based…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3170-2026·2026-09-23
GE Healthcare Recalls Workflow Core Services V8 Due to Data Association Errors
GE Healthcare is recalling Workflow Core Services V8 because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
Product
Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administration, common configuration management for consuming applications, All versions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3171-2026·2026-09-23
GE Healthcare Recalls Core Services Hub V8 Due to Data Association Errors
GE Healthcare is recalling Core Services Hub V8 software because historical imaging data may be incorrectly associated with the wrong patient, potentially leading to misdiagnosis.
Product
Core Services Hub V8, a set of backend services including Cross Enterprise (XE) and Workflow Core (WFC) services that enables enterprise imaging workflows, All versions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3161-2026·2026-09-23
ICU Medical Recalls IV Sets with Potential Drip Chamber Discoloration
ICU Medical is recalling IV sets with drip chambers due to potential black specks and particulate matter in the fluid path.
Product
IV Sets with drip chambers
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3176-2026·2026-09-23
Happiest Baby SNOO Sleep Sacks Recalled for Lack of FDA Review
Happiest Baby, Inc. is recalling SNOO Sleep Sacks because they have not been reviewed for safety and effectiveness by the FDA.
Product
Happiest Baby, Inc. SNOO Sleep Sack, X-Large Model/Catalog Number: S2101-501 S2101-508-11 S2101-508-3 S2101-508-4 S2101-508-5 S2101-508-6 S2101-508-7 S2101-512 S2101-513 S2101-532 S2101-533 S2101-534 S2101-535 S2101-536 S2101-541 S2101-551 S2102-508-10 S2102-508-9 S2103-501…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3193-2026·2026-09-23
Mirion Captus 4000e Thyroid Uptake System Recalled for Spring Arm Failure
Mirion Technologies is recalling 783 Captus 4000e Thyroid Uptake Systems because a tension bolt may fail, causing the spring arm to fall unexpectedly.
Product
Captus 4000e Thyroid Uptake System, Models: 1. 5430-30151, 2. 5430-30152, 3. 5430-30154;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3212-2026·2026-09-23
ICU Medical Recalls CADD Yellow Medication Cassette Reservoirs Due to Leakage
ICU Medical is recalling 185,688 CADD Yellow Medication Cassette Reservoirs because they may leak medication at the connector joint, potentially interrupting therapy or causing exposure to harmful agents.
Product
CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes: 21-7600-24, 21-7609-24 OUS Product Codes: 21-7609-24 21-7600-24 21-7600-24 21-7600-24 21-7609-24 21-7609-24 21-7600-24 21-7600-24 21-7609-24 21-7609-24 21-7600-24 21-7600-24…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3179-2026·2026-09-23
Embecta Medical Recalls Nano Pro Pen Needles Distributed as Commercial Devices
Embecta Medical II LLC is recalling Nano Pro Un-Cannulated Demo Samples because investigational-use-only pen needles were inadvertently distributed as commercially marketed devices.
Product
EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100
Category
Medical Device
Distribution
Distributed nationwide