The Recall Desk

State

Michigan product recalls

20,324 recalls have nationwide distribution and so reach Michigan. 0 additional recalls listed Michigan specifically in their distribution scope.

About recalls in Michigan

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Michigan consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14251–14275 of 20324

  • HighNHTSA·22V687000·2023-02-09

    2022 Volkswagen Taos Engine Stall Software Safety Recall

    Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.

    Product
    VOLKSWAGEN — 2022 VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23724·2023-02-09

    WeeSprout Baby Sleep Sacks Recalled Due to Choking Hazard

    WeeSprout baby sleep sacks are being recalled because the zipper can detach, posing a choking hazard to infants. The company has received 17 reports of zipper detachment but no injuries have been reported.

    Product
    Baby Sleep Sacks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0246-2023·2023-02-08

    First Aid Kit with Burn Cream Recalled for Bacterial Contamination

    GFA Production is recalling Adventure First Aid 1.0 kits containing Easy Care After Burn Cream due to confirmed bacterial contamination found in FDA testing. The affected product was distributed nationwide and in Canada.

    Product
    Adventure First Aid 1.0, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0213
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0244-2023·2023-02-08

    Easy Care first aid burn cream recalled for microbial contamination

    Easy Care first aid burn cream distributed nationwide and in Canada is recalled due to FDA-detected contamination with Bacillus lichenformis and Bacillus sonorensis. The product should not be used.

    Product
    Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and lidocaine hydrochloride 0.5%), 0.9 g (0.03 oz) packets packaged in boxes of 10, Treatment for Burns, Made in China for Adventure Ready Brands, 944 Industrial Park Rd., Littleton, NH 03561, NDC 90107-0210, Product # 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0250-2023·2023-02-08

    Easy Care First Aid Kit Recalled for Bacterial Contamination

    GFA Production is recalling Easy Care First Aid Kits distributed nationwide and in Canada due to bacterial contamination of included After Burn Cream packets. The FDA confirmed the presence of Bacillus lichenformis and Bacillus sonorensis.

    Product
    Easy Care First Aid Class A ANSI 25 Person, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2150
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0252-2023·2023-02-08

    CVS First Aid Home Burn Cream Packets Recalled for Bacterial Contamination

    CVS First Aid Home, First Aid Kit burn cream packets have been recalled due to bacterial contamination. The product contains Bacillus lichenformis and Bacillus sonorensis bacteria, creating a risk when applied to wounds or burns.

    Product
    CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 2980-0700
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0249-2023·2023-02-08

    Easy Care First Aid Kits Recalled for Bacterial Contamination

    GFA Production is recalling Easy Care First Aid 10 Person First Aid Kits because the included After Burn Cream packets are contaminated with Bacillus bacteria. Contamination was identified through FDA laboratory testing.

    Product
    Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2128
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0247-2023·2023-02-08

    FDA Recalls First Aid Cream Packets Over Bacterial Contamination

    The FDA is recalling Adventure First Aid 1.5 first aid kits due to bacterial contamination found in the included burn cream packets. The contamination was identified through FDA laboratory testing.

    Product
    Adventure First Aid 1.5, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0212
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V663000·2023-02-08

    Coach House Platinum II recreational vehicle window adhesive failure recall

    Coach House is recalling 2019-2022 Platinum II and 2022 Platinum recreational vehicles due to window adhesive failure. The adhesive bonding the window vent may fail, potentially causing detachment and increasing crash or injury risk.

    Product
    COACH HOUSE — 2021 COACH HOUSE PLATINUM II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0962-2023·2023-02-08

    CADD Administration Set recall: medication underdelivery and false alarms

    Smiths Medical is recalling 1.6 million CADD Infusion System Administration Sets due to tubing occlusion causing medication underdelivery and false alarm conditions affecting patients worldwide.

    Product
    CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0245-2023·2023-02-08

    First Aid Kit Product Recalled Due to Bacterial Contamination

    A first aid kit containing topical burn cream has been recalled due to bacterial contamination with Bacillus species. The product (Lot W06I20) was distributed nationwide and in Canada.

    Product
    Adventure Marine 150, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 1015-0150
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0966-2023·2023-02-08

    CADD Administration Sets recall for delivery failure and false alarms

    Smiths Medical is recalling CADD Administration Sets due to potential tubing occlusion causing medication underdelivery and false alarm errors. The FDA classified this as a Class I recall affecting nearly 48 million units worldwide.

    Product
    CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24, 3) REF 21-7302-24, 4) REF 21-7308-24, 5) REF 21-7309-24, 6) REF 21-7310-24, 7) REF 21-7322-24, 8) REF 21-7323-24, 9) REF 21-7324-24, 10) REF 21-7333-24, 11) REF 21-7343-24, 12) REF 21-7346-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0929-2023·2023-02-08

    SARS-CoV-2 Antigen Rapid Test Kits Recalled for Lack of FDA Authorization

    Universal Meditech Inc. is recalling approximately 56,300 SARS-CoV-2 Antigen Rapid Test Kits distributed without FDA approval, clearance, or Emergency Use Authorization. Products were distributed nationwide in California and Texas.

    Product
    Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green and white box under the brand DiagnosUS, and, White box without brand name labeled as "SARS -COV-2 ANTIGEN DEVELOPMENT MADE IN USA ORAL SWAB TES
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0253-2023·2023-02-08

    Easy Care First Aid Kit Recalled for Microbial Contamination

    The FDA is recalling Easy Care First Aid kits containing After Burn Cream due to microbial contamination. The affected product was distributed nationwide and in Canada with lot number W06H15 (expiration August 15, 2024).

    Product
    Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2131
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0963-2023·2023-02-08

    CADD Infusion Administration Sets Recalled for Tubing Occlusion and False Alarms

    Smiths Medical is recalling CADD Administration Sets for two issues: tubing may become blocked, preventing medication delivery, and devices may show false alerts about disposable attachment status.

    Product
    CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4) REF 21-7321-24, 5) REF 21-7322-24, 6) REF 21-7323-24, 7) REF 21-7324-24, 8) REF 21-7333-24, 9) REF 21-7336-24, 10) REF 21-7339-24, 11) REF 21-7343-24, 12) REF 21-7349-24,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0964-2023·2023-02-08

    CADD Infusion Administration Sets Recalled for Delivery Failure and Alarms

    FDA recalls 726,878 CADD Infusion Administration Sets due to potential tubing occlusion causing delivery failure and false alarm warnings.

    Product
    CADD Administration Set, List Numbers: a) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24, d) REF 21-7308-24JP, e) REF 21-7309-24JP. Computerized Ambulatory Delivery Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0965-2023·2023-02-08

    CADD Infusion Administration Set Recalled for Delivery Failure and False Alarms

    Smiths Medical is recalling CADD Administration Sets due to tubing occlusion that can prevent medication delivery and false pump alarms. This FDA Class I recall affects 214,668 units worldwide.

    Product
    CADD Administration Set, List Numbers: a) REF 21-7600-24, b) REF 21-7609-24, c) REF 21-7624-24, d) REF 21-7649-24, e) REF 21-7600-24JP, f) REF 21-7609-24JP, g) REF 21-7624-24JP, h) REF 21-7649-24JP Computerized Ambulatory Delivery Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0248-2023·2023-02-08

    FDA Recalls Easy Care First Aid Kits for Bacterial Contamination

    GFA Production's Easy Care First Aid 25 Person kits are being recalled nationwide due to contamination with Bacillus bacteria. The affected first aid cream packets could pose a risk if applied to open wounds.

    Product
    Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2129
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0251-2023·2023-02-08

    FDA Recalls Easy Care First Aid Kit for Bacterial Contamination

    The FDA is recalling Easy Care First Aid Kits with contaminated After Burn Cream packets distributed nationwide and in Canada. Lab testing identified Bacillus lichenformis and Bacillus sonorensis contamination.

    Product
    Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2132
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1029-2023·2023-02-08

    MEDLINE procedural trays recalled for potential sterile packaging breach

    MEDLINE is recalling procedural trays because sterile blades within the kits could puncture the outer foil packaging, potentially breaching the sterile barrier.

    Product
    Non-sterile procedural trays labeled as CRANI, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2023·2023-02-08

    SynCardia Total Artificial Heart System Recalled for Cannula Tears

    SynCardia Systems is recalling its Total Artificial Heart System due to reported tears in the cannula caused by wear and tear stress. Approximately 1,732 systems worldwide are affected.

    Product
    SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V668000·2023-02-08

    Land Rover seat belt retractor defect affects child restraint security

    Land Rover is recalling certain 2020-2022 vehicles because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly. This can increase the risk of injury during a crash.

    Product
    LAND ROVER — 2021 LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1047-2023·2023-02-08

    Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk

    Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.

    Product
    MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1048-2023·2023-02-08

    GORE CARDIOFORM Septal Occluder Recalled for Incomplete Quality Documentation

    W L Gore & Associates is recalling 14 units of the GORE CARDIOFORM Septal Occluder (GSX0030A) due to incomplete quality test documentation. The missing verification of device release could pose a potential risk of device failure and serious complications.

    Product
    GORE CARDIOFORM Septal Occluder, REF: GSX0030A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·23115·2023-02-08

    Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk

    Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.

    Product
    Fabuloso Multi-Purpose Cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide