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MICHIGAN HERBAL REMEDIES

MICHIGAN HERBAL REMEDIES Recalls

All product recalls associated with MICHIGAN HERBAL REMEDIES.

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Recall Summary

Total Recalls

1000

Past Year

589

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 4261–4280 of 10393 recalls

Pathway Hemp Oil Drops (Michigan Herbal) – Lead contamination (2020)

Undeclared Allergen

Chemical contamination: product contains elevated levels of undeclared lead.

Class IHigh

FDAJun 18, 2020Nationwide• MICHIGAN HERBAL REMEDIES

LoFric Origo Catheter (Wellspect) – Potential Product Defect (2020)

Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheter s distal tip.

FDAJun 17, 2020AL, AZ, CA +19 more• Wellspect HealthCare (Division of DENTSPLY IH AB) Aminogatan 1 Molndal Sweden

Office Chairs (HON) – Fall Hazard (2020)

This recall involves HON's Gateway office chairs with model numbers HGTMM and HGV1MM and manufactured from February 2019 through February 2020. It also involves the Maxon MXMO series chairs, model numbers M-SEMO201 and M-SEMX101. The manufacturer's name, model number and manufacture date are printed on a label located on the underside of the seats. The office chairs have a black mesh see-through back and a five-star base with wheels. HON or Maxon is printed on a label underneath the seat.

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CPSCJun 17, 2020Nationwide• The HON Company LLC, of Muscatine, Iowa

DxA 5000 (Beckman Coulter) – Sample ID Confusion (2020)

The DxA 5000 instructions for use may be confusing regarding the re-use of sample IDs. Beckman Coulter has received complaints where the re-use of sample barcodes were not being detected by the system .

FDAJun 17, 2020Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munich Germany

LoFric Origo Tiemann Catheter (Wellspect) – Potential Product Defect (2020)

Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheters distal tip.

FDAJun 17, 2020AL, AZ, CA +19 more• Wellspect HealthCare (Division of DENTSPLY IH AB) Aminogatan 1 Molndal Sweden

MatrixMIDFACE Screws (Synthes) – Incorrect Screw Packaging (2020)

One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm).

FDAJun 16, 2020IN• Synthes Produktions GmbH Eimattstrasse

Childrens Dimetapp Cold & Cough (Glaxosmithkline) – Defective Dosing Cup (2020)

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Class IIModerate

FDAJun 16, 2020Nationwide• Glaxosmithkline Consumer Healthcare Holdings

Childrens Robitussin Honey Cough (Glaxosmithkline) – Defective Dosing Cup (2020)

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Class IIModerate

FDAJun 16, 2020Nationwide• Glaxosmithkline Consumer Healthcare Holdings

Metformin Extended Release (Harvard Drug) – NDMA Impurity (2020)

CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity above the established levels.

Class IIModerate

FDAJun 12, 2020Nationwide• The Harvard Drug Group

Raw Macadamia Nuts (NOW) – Salmonella Contamination (2020)

Salmonella

The product tested positive for Salmonella enterica.

Class IHigh

FDAJun 12, 2020Nationwide• NOW Health Group Inc.

Irinotecan Injection (Hikma Pharmaceuticals) – Crimp Defect (2020)

Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.

Class IIModerate

FDAJun 11, 2020Nationwide• Hikma Pharmaceuticals USA Inc.

Irinotecan Injection (Hikma Pharmaceuticals) – Crimp Defect (2020)

Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.

Class IIModerate

FDAJun 11, 2020Nationwide• Hikma Pharmaceuticals USA Inc.

Nabumetone Tablets (American Health Packaging) – Incomplete Labeling (2020)

Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with the accompanying Medication Guide was not included on the carton label.

Class IIILow

FDAJun 10, 2020Nationwide• American Health Packaging

Axis RV (Thor Motor Coach) – Window Glass Adhesive Issue (2020)

Thor Motor Coach (TMC) is recalling certain 2020-2021 ACE, 2021 Four Winds and 2020 Gemini, Axis, Compass, Delano, Windsport, Hurricane, Outlaw, and Vegas motorhomes. The adhesive bond between the glass and the metal hinge frame of the frameless windows may fail which would then allow the glass to detach and fall out.

NHTSAJun 9, 2020Nationwide• THOR MOTOR COACH

Open Range Trailer (Highland Ridge) – Window Adhesive Failure (2020)

Highland Ridge RV (Highland Ridge) is recalling certain 2020 Ridge, Open Range, and Silverstar recreational trailers. The adhesive bond between the glass and the metal hinge frame of the frameless crank out vent and egress windows may fail which would then allow the glass to detach and fall out.

NHTSAJun 9, 2020Nationwide• HIGHLAND RIDGE TT

Microstream CO2 Extension (Philips) – Monitor Compatibility Issue (2020)

Affected M3015A extensions are incompatible with the lntelliVue X3 Patient Monitor (Model No. 867030) and lntelliVue MMX multi-measurement server (Model No. 867036).If they are connected to a host monitor, communication with the X3 or MMX could be disrupted, resulting in a loss of monitoring on the host monitor.

FDAJun 8, 2020Nationwide• Philips North America, LLC

Atellica CH Calibrator (Siemens) – Calibration Error (2020)

Calibration errors have been observed with the Total and Direct Bilirubin assays when using Chemistry Calibrator lot 534177 for ADVIA Chemistry and lot 534179 for Atellica CH.

FDAJun 5, 2020Nationwide• Siemens Healthcare Diagnostics, Inc.

ADVIA Chemistry Calibrator (Siemens) – Calibration Error (2020)

Calibration errors have been observed with the Total and Direct Bilirubin assays when using Chemistry Calibrator lot 534177 for ADVIA Chemistry and lot 534179 for Atellica CH.

FDAJun 5, 2020Nationwide• Siemens Healthcare Diagnostics, Inc.

TEM Tube Set (Richard Wolf) – Tube Diameter Mismatch (2020)

Tube material of a smaller diameter was used.

FDAJun 5, 2020CA, DE, IN• Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany

Solara CRT-P MRI (Medtronic) – Communication Interruption (2020)

There is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i.e., battery measurements, Capture Management", Atrial Lead Position Check", EffectivCRT" algorithms, and AdaptivCRT"). This rare interaction results in temporary suspension of automatic threshold testing and output adjustments, and suspension of auto-optimization of CRT therapy. The issue is unlikely to result in clinical impact to the patient, and features are restored upon next programmer device interrogation or presence of a magnet.

FDAJun 4, 2020Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)