Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

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 ↗

Home
/
Brands
/
Calvin Scott & Company, Inc.

Calvin Scott & Company, Inc. Recalls

All product recalls associated with Calvin Scott & Company, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

91

Most Recent

Dec 2025

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 3701–3720 of 10937 recalls

Hydrochlorothiazide 50mg (Calvin Scott) – Light Sensitivity Packaging (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

Phentermine HCL GrayYellow Capsules (Calvin Scott) – Light Sensitivity Risk (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

Phentermine HCL White/Blue Speckled Tablets (Calvin Scott) – Light Sensitivity Risk (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

1...184 185186187 188...547

Page 186 of 547Next

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

Hydrochlorothiazide 25mg (Calvin Scott) – Light Sensitivity Packaging (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

Phentermine HCL Yellow Caps (Calvin Scott) – Light Sensitivity Risk (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

Topiramate Tabs (Calvin Scott) – Light Sensitivity Risk (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

Thyroid 1 Grain Tablets (Calvin Scott) – Light Sensitivity Risk (2020)

CGMP Deviations: Light sensitive drug products repackaged in transparent/partially transparent pouches.

Class IIModerate

FDAJul 27, 2020Nationwide• Calvin Scott & Company, Inc.

DABRA Excimer Laser (Ra Medical) – mounting stability (2020)

Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury.

FDAJul 24, 2020Nationwide• Ra Medical Systems, Inc.

Garden Cut Organic Coleslaw (Indianapolis Fruit) – plastic pieces (2020)

Foreign material, pieces of plastic found in finished product

Class IIModerate

FDAJul 24, 2020IL, IN, MI +3 more• Indianapolis Fruit Company, Inc.

Ranger Off-Road Vehicles (Polaris) – crash risk (2020)

This recall involves Model Year 2020 Ranger XP 1000 and Ranger CREW XP 1000 Off-Road Vehicles, Model Years 2019-2020 PRO XD 4000D UTVs, Model Year 2019 PRO XD 2000D, and Model Year 2020 Bobcat UV34 and UV34XL UTVs. The vehicles were sold in maroon, black, sand, green, orange, blue, camo, gray and white colors and have two or four seats. For PRO XD and Ranger models, "POLARIS" is stamped on the front grille and "POLARIS PRO XD" or "Ranger" is printed on the sides of the rear cargo area. For Bobcat models, "Bobcat" is printed on the sides of the rear cargo area. The VINs included in this recall can be found stamped into the left rear vehicle frame below the cargo box. The following model names are included in this recall: YEAR MODEL NAME 2019 PRO XD 4000D 2019 PRO XD 2000D 2020 PRO XD 4000D 2020 Ranger XP 1000 2020 Ranger XP 1000 Crew 2020 Bobcat UV34 2020 Bobcat UV34XL

CPSCJul 23, 2020Nationwide• Polaris Industries Inc., of Medina, Minn.

CombiDiagnost R90 (Philips) – software value lock (2020)

Philips has become aware of a software issue, where the kV and mA values are not locked immediately but change when the collimator shutter position is changed directly after the Lock-In command. This software issue leads to an over or under exposed image.

FDAJul 22, 2020Nationwide• Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany

Ezycare Face Mask (Beyond White) – medical use mislabeling (2020)

Disposable face masks labeled as non-medical were distributed to customers expecting medical use face masks.

FDAJul 21, 2020Nationwide• BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

NobelReplace Conical Connection (NOBEL BIOCARE) - Implant Measurement Error (2020)

Dental implant cap label may incorrectly indicate implant measurements 5.0x8mm. Actual implant measurements are 4.3x10mm. If not noticed prior to implant placement, this could lead to: 1) A second surgical procedure; 2) Implant replacement; 3) If placed in posterior lower jaw, the implant may damage the inferior alveolar nerve canal or perforate a small artery requiring immediate implant removal.

FDAJul 20, 2020Nationwide• NOBEL BIOCARE SERVICES AG Balz-zimmermannstrasse 7 Kloten Switzerland

Proteus 235 (Ion Beam Applications) - Treatment Resumption Issue (2020)

IBA became aware of an issue to resume aborted irradiations because the plan to complete the treatment cannot be loaded.

FDAJul 17, 2020VA• Ion Beam Applications S.A. Chemin Du Cyclotron 3 Louvain-la-neuve Belgium

Match Point System (Materialise) - Procedure Side Mislabeling (2020)

The procedure side indicated in the top header of the Shoulder Case Planning Report incorrectly indicated the procedure side as "Left" for surgical plans for a "right" procedure side.

FDAJul 17, 2020Nationwide• Materialise N.V. Technologielaan 15 Heverlee Belgium

Restore Clinician Programmer (Medtronic) - Software Compatibility Issue (2020)

The original version of the A71100 Restore Clinician Programmer Application has been identified to have a compatibility issue with some legacy clinician programmer software resulting in the programmer having an inability to establish communication with the implanted neurostimulators.

FDAJul 17, 2020Nationwide• Medtronic Neuromodulation

Cytocell LPH533-A NUP98 Probe (Cytocell) - False Positive Risk (2020)

A low risk of a false positive result being issued with a laboratory developed test (LDT) that utilizes the LPH533-A NUP98 Distal Probe Green.

FDAJul 17, 2020Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

AXYS Snowmobiles (Polaris) – Fire Hazard (2020)

This recall involves all Model Year 2015-2020 600cc and 800cc AXYS Trail Performance and Crossover snowmobiles with the following model names. The model year and VIN are stamped on the right side of the tunnel. Polaris and the model name are printed on both sides of the hood and on the side panels of the vehicles. Model Year Model Name 2015 RUSH SWITCHBACK 2016 RUSH SWITCHBACK 2017 RMK RUSH SWITCHBACK VOYAGEUR 2018 RMK RUSH SWITCHBACK VOYAGEUR 2019 INDY RMK RUSH SWITCHBACK VOYAGEUR 2020 INDY RMK RUSH SWITCHBACK VOYAGEUR

CPSCJul 16, 2020Nationwide• Polaris Industries Inc., Medina, Minn.

BRAINLAB Curve (Brainlab) - Calibration Error (2020)

Incorrect manufacturer calibration

FDAJul 16, 2020CA, RI, TX• Brainlab AG Olof-palme-str. 9 Munich Germany

BRAINLAB Kick 2 (Brainlab) - Calibration Error (2020)

Incorrect manufacturer calibration

FDAJul 16, 2020CA, RI, TX• Brainlab AG Olof-palme-str. 9 Munich Germany