Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
MORGAN MOTOR COMPANY

MORGAN MOTOR COMPANY Recalls

All product recalls associated with MORGAN MOTOR COMPANY.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 2941–2960 of 25002 recalls

Morgan Super 3 (Morgan Motor Company) – Pedal Box Welding Defect (2024)

Morgan Motor Company Limited (MMC) is recalling certain 2023 Super 3 motorcycles. The pedal box housing may have been improperly welded, which can result in the hydraulic seal between the hose and master cylinder breaking, causing a loss of brake function.

High

NHTSAJan 17, 2024Nationwide• MORGAN MOTOR COMPANY

Mexican Style Quinoa Salad (Hans Kissle) – Undeclared Allergens (2024)

Undeclared Soy

contains undeclared soy and egg

Class IHigh

FDAJan 17, 2024ME, MA, NH +2 more• Hans Kissle Company, LLC

InstaClear Lens Cleaner (Olympus) – Instructions Variation (2024)

Japanese IFU version had slightly different language and illustrations from the English IFU, which could contribute to the tip and plate falling off. In order to maintain consistency globally, the Japanese IFU will be updated to reflect the instructions in the English IFU

1...146 147148149 150...1251

Page 148 of 1251Next

Low

FDAJan 16, 2024Nationwide• Olympus Corporation of the Americas

MIC Gastric-Jejunal Feeding Tube (Avanos) – Syringe Recall (2024)

MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled syringe subsequently recalled by Nurse Assist.

High

FDAJan 16, 2024Nationwide• Avanos Medical, Inc.

HLS Set Advanced (Maquet) – Sterile Barrier Compromise (2024)

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

High

FDAJan 16, 2024Nationwide• Maquet Medical Systems USA

HLS Set Advanced (Maquet) – Sterile Barrier Compromise (2024)

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

High

FDAJan 16, 2024Nationwide• Maquet Medical Systems USA

W&H Surgical Handpiece (W&H) – Laser Marking Error (2024)

1:2 speed increasing surgical handpieces have been incorrectly laser marked during production. The specific laser marking should read 1:2, but instead it reads 1:1 on the body of the handpiece

Low

FDAJan 16, 2024Nationwide• W & H DENTALWERK BUERMOOS GMBH Ignaz Glaser Strase 53 53 IGNAZ-GLASER-STRASSE BUERMOOS Austria

Water Filter MAJ-2318 (Olympus) – Incorrect Assembly (2024)

Water filter may have been assembled incorrectly, resulting in unfiltered tap water being used for reprocessing. This may expose a patient to a potentially contaminated device, presenting a risk of infection or sepsis.

High

FDAJan 16, 2024Nationwide• Olympus Corporation of the Americas

Phenoxybenzamine Hydrochloride Capsules (Amneal) – Impurity Specification (2024)

Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.

Class IIModerate

FDAJan 15, 2024Nationwide• Amneal Pharmaceuticals of New York, LLC

Directional Laser Probe (D.O.R.C.) – Fiber Extension Problem (2024)

When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.

Moderate

FDAJan 15, 2024Nationwide• D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Scheijdelveweg 2 Zuidland Netherlands

Notoginseng Gout Granule (8th Ave Pharmacy) – Undeclared Drugs (2024)

Undeclared Allergen

Product contains undeclared Diclofenac and Dexamethasone Acetate

Class IIModerate

FDAJan 14, 2024AL, CO, FL +22 more• 8TH AVE PHARMACY

3M Specialty Blade Assembly (3M) – Burn Risk (2024)

Fire/Burn Risk

3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in minor injury: " Do not use on injured skin. " Do not leave clipper running unused in air without applying to skin for more than 1 minute as blade temperature may exceed 41C (105.8F). " Do not leave the clipper blade applied to the same location on the patient s skin for longer than 1 second as potential injury may occur; continuous motion of the clipper during use is required. Note: If clipper is left running unused in air for 10 minutes without applying to skin, the Model 9690 blade maximum temperature may reach 60C (140F) and the Model 9660 blade maximum temperature may reach 77C (170.6F)."

Low

FDAJan 12, 2024Nationwide• 3M Company Health Care Business 3m Center