State

Michigan product recalls

20,308 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.

13201–13225 of 20308

ModerateFDA (Drugs)·D-0768-2023·2023-05-31
Fentanyl Buccal Tablets 400mcg missing or incorrect package insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 400mcg due to incorrect or missing package inserts in affected cartons distributed nationwide. No illnesses have been reported.
Product
Fentanyl Buccal Tablets CII, 400mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-636-28
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0767-2023·2023-05-31
Fentanyl Buccal Tablets Recalled for Missing or Incorrect Package Insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets (200mcg) due to missing or incorrect package inserts. Patients should contact their healthcare provider if they have affected product.
Product
Fentanyl Buccal Tablets CII, 200mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-635-28
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1632-2023·2023-05-31
Siemens Atellica CH Toxicology Calibrator Reassignment Due to Positive Bias
Siemens Healthcare Diagnostics is reassigning Atellica CH Toxicology Calibrators due to a positive bias. The affected calibrators were distributed in the US and internationally across multiple countries.
Product
Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica¿ CH Toxicology Calibrator (TOX CAL) is for in vitro diagnostic use in calibrating the Acet, ETOH and Sal assays using the Atellica¿ CH Analyzer Siemens Material Number (SMN): 11099440
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1479-2023·2023-05-31
Fluoroscopic imaging system may display incorrect radiation dose readings
Siemens Luminos Agile Max fluoroscopic imaging systems may occasionally display incorrect radiation dose information under certain unlikely circumstances. The manufacturer states there is no impact on clinical workflow or diagnosis. The error only occurs in systems with a second overhead X-ray tube.
Product
Luminos Agile Max (VE10, VF10, VF11)
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0756-2023·2023-05-31
Methylprednisolone Acetate Injectable Suspension recalled for NDC carton labeling error
Amneal Pharmaceuticals recalls Methylprednisolone Acetate Injectable Suspension due to incorrect NDC number on product cartons. The typographical error appears on secondary packaging only; the medication vial itself is unaffected.
Product
Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular, Intrasynovial and Soft Tissue Injection Only, Not for Intravenous Use, 1 mL Single Dose Vial, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Parenteral Unit, Ahmedabad 382213, India, Amneal Phar
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0769-2023·2023-05-31
Fentanyl Buccal Tablets 600mcg Recalled for Incorrect or Missing Package Insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 600mcg due to incorrect or missing package inserts in 1,908 units distributed nationwide across multiple lot numbers.
Product
Fentanyl Buccal Tablets CII, 600mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-637-28
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0766-2023·2023-05-31
Fentanyl Buccal Tablets recalled due to missing or incorrect package insert
Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 100mcg due to incorrect or missing package inserts in affected cartons. Patients should verify proper labeling or contact their pharmacy.
Product
Fentanyl Buccal Tablets CII, 100mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-634-28
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0770-2023·2023-05-31
Fentanyl buccal tablets recalled due to incorrect or missing package insert
Teva Pharmaceuticals USA Inc is recalling Fentanyl Buccal Tablets 800mcg due to incorrect or missing package inserts. The recall affects 3,032 units distributed nationwide.
Product
Fentanyl Buccal Tablets CII, 800mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-638-28
Category
Drug
Distribution
Distributed nationwide
HighCPSC·23761·2023-05-25
Bunch Bikes Recalls The Preschool Electric Bicycles Due to Excess Lead Paint
Bunch Bikes is recalling about 150 units of The Preschool Electric Bicycles sold online from April 2020 through December 2022 because the paint contains lead levels exceeding the federal ban. Lead is toxic if ingested by young children and can cause adverse health effects.
Product
The Preschool Electric Bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23210·2023-05-25
Janod Sweet Cocoon Activity Tables Recalled for Choking Hazard
Juratoys is recalling about 5,080 Janod Sweet Cocoon Activity Tables because a detachable silver metal bell poses a choking hazard to children 12 months and older. Consumers should stop using the tables and contact Juratoys for a free repair kit.
Product
Janod Sweet Cocoon Activity Tables
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·23762·2023-05-25
The Good and the Beautiful Math Boxes Recalled Due to Laceration Hazard
The Good and the Beautiful is recalling Math 1 and Math 3 boxes with metallic whiteboards because the attached whiteboards can detach and cause lacerations. Four minor laceration injuries have been reported.
Product
The Good and the Beautiful Math 1 and Math 3 Boxes with metallic whiteboards
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0920-2023·2023-05-24
Gold Medal Flour Recalled Nationwide for Potential Salmonella Contamination
General Mills is recalling Gold Medal Bleached All Purpose Flour nationwide due to potential Salmonella contamination. Approximately 271,454 bags are affected.
Product
Gold Medal Bleached All Purpose Flour, Enriched, Presifted, packaged in the following sizes: 1. Net Wt 32 oz (2lb) 907g, UPC 0 16000-10710 6; and 2. Net Wt 5lb (2.26kg), UPC 0 16000-10610 9. Dist. By General Mills Sales, Inc., Minneapolis, MN 55440.
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1447-2023·2023-05-24
Draeger VentStar Anesthesia Breathing Circuit Connections May Detach
Draeger Medical recalls VentStar Anesthesia (N) 180 breathing circuits. Glued connections can loosen or detach during ventilation, potentially creating a critical disconnection risk.
Product
VentStar Anesthesia (N) 180, MP00333
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1440-2023·2023-05-24
Draeger VentStar Basic ventilator breathing circuit connections may detach during use
Draeger Medical is recalling 325 VentStar Basic (P)180 ventilators because glued breathing circuit connections can become loose before or during ventilation, potentially causing partial or complete detachment of circuit pieces.
Product
VentStar Basic (P)180, MP00351
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1444-2023·2023-05-24
Anesthesia Ventilator Breathing Circuit Connections May Detach During Use
Draeger Medical is recalling 130 units of the VentStar Anesthesia WT ventilator due to a defect where glued breathing circuit connections may loosen or detach during ventilation, potentially compromising anesthesia delivery.
Product
VentStar Anesthesia WT (P)180, MP00374
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1450-2023·2023-05-24
Draeger VentStar Breathing Circuit Connections May Loosen During Use
Draeger Medical is recalling the VentStar Bag Set because glued connections on the breathing circuit can become loose or detach during ventilation, potentially compromising respiratory support.
Product
VentStar Bag Set (N) 110, MP00383
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1456-2023·2023-05-24
Breathing circuit component connections may become loose during ventilation
Draeger Medical recalls ID Coax 180 breathing circuit components due to glued connections that can become loose or detach during ventilation.
Product
ID Coax 180, MP03375
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1448-2023·2023-05-24
VentStar Basic Ventilator Recall: Risk of Breathing Circuit Detachment
Draeger Medical is recalling 1,725 VentStar Basic ventilators because glued breathing circuit connections can become loose and detach before or during ventilation. This may disrupt patient breathing support.
Product
VentStar Basic (N) 180, MP00353
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1451-2023·2023-05-24
VentStar Coax breathing circuit connections recalled for detachment risk
Draeger Medical is recalling VentStar Coax (P) 150 breathing circuit components due to potentially loose glued connections that could detach during ventilation, affecting 280 units distributed nationwide.
Product
VentStar Coax (P) 150, MP00379
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1457-2023·2023-05-24
Ventstar Coax 230 breathing circuit connections can detach during ventilation
The FDA is recalling Draeger Medical's Ventstar Coax 230 breathing circuit components due to glued connections that can become loose and detach during ventilation, potentially compromising patient breathing support.
Product
Ventstar Coax 230, MP03376
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1455-2023·2023-05-24
Ventstar Coax 180 Ventilator Breathing Circuit Connections May Detach
Draeger Medical is recalling 18,160 Ventstar Coax 180 ventilators because glued breathing circuit connections can become loose and detach during use, potentially disrupting oxygen delivery.
Product
Ventstar Coax 180, MP03374
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1442-2023·2023-05-24
VentStar Watertrap Breathing Circuit Connections May Detach During Use
Draeger Medical recalls VentStar Watertrap (P) 180 breathing circuit equipment because glued connections can become loose or detach before or during ventilation.
Product
VentStar Watertrap (P) 180, MP00361
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1452-2023·2023-05-24
Anesthesia Circuit Kit Coax 1 Recall: Breathing Circuit Connections May Loosen or Detach
Draeger Medical is recalling Anesthesia Circuit Kit Coax 1 (MP02730) because glued breathing circuit connections can become loose or detach during ventilation, affecting the breathing circuit's function.
Product
Anesthesia Circuit Kit Coax 1, MP02730
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1453-2023·2023-05-24
Anesthesia Circuit Kit Coax 3 Connections May Detach During Ventilation
Draeger Medical is recalling Anesthesia Circuit Kit Coax 3 units because glued connections can become loose or detach before or during ventilation. The recall covers 329,294 units distributed nationwide.
Product
Anesthesia Circuit Kit Coax 3, MP02732
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1458-2023·2023-05-24
Anesthesia Set Coax 180 Breathing Circuit Connection Risk
Draeger Medical is recalling the Anesthesia Set Coax 180 because glued breathing circuit connections can become loose during ventilation, causing partial or complete detachment.
Product
Anesthesia Set Coax 180, MP03384
Category
Medical Device
Distribution
Distributed nationwide