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Professional Disposables International, Inc

Professional Disposables International, Inc Recalls

All product recalls associated with Professional Disposables International, Inc.

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Recall Summary

Total Recalls

1000

Past Year

144

Class I (Serious)

154

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 341–360 of 1339 recalls

PDI Povidone-Iodine Prep Pad Large (Professional Disposables) – Subpotent Specification (2021)

SubPotent: Out of Specification

Class IIModerate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

PDI Povidine Iodine Swabstick (Professional Disposables) – Subpotent Specification (2021)

SubPotent: Out of Specification

Class IIModerate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

PDI Duo-Swab Povidone-Iodine Scrub Swabstick (Professional Disposables) – Subpotent Specification...

SubPotent: Out of Specification

Class II

1...16 171819 20...67

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Moderate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

PDI Povidone-Iodine Cleansing Scrub Swabstick (Professional Disposables) – Subpotent Specificatio...

SubPotent: Out of Specification

Class IIModerate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

PDI Povidone-Iodine Prep Pad Medium (Professional Disposables) – Subpotent Specification (2021)

SubPotent: Out of Specification

Class IIModerate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

PDI Povidone-Iodide Cleansing Scrub Swabstick (Professional Disposables) – Subpotent Specificatio...

SubPotent: Out of Specification

Class IIModerate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

Acetaminophen Extra Strength Tablets (LNK) – Incorrect Labeling (2021)

Labeling: Not Elsewhere Classified The primary label contains the words "enteric coated" but the tablet is not enteric coated and should only say 'coated tablet'

Class IIILow

FDAJul 7, 2021IN, PA• LNK International, Inc.

Eight Medical International BV Laan Van Hildernisse-Noord 2a Bergen Op Zoom Netherlands: Recirculator 8.0s Disposable Lavage Kit (product code num...

The patient may be exposed to potential aluminum ion release during warming therapy under certain use conditions.

FDAJun 4, 2021Nationwide• Eight Medical International BV Laan Van Hildernisse-Noord 2a Bergen Op Zoom Netherlands

Sodium Potassium Hydroxide (Pro Supply) – Safety Concern (2021)

Fire/Burn Risk

This recall involves Pro Supply Outlet sodium and potassium hydroxide products sold in two-pound rigid white plastic jars with continuous thread caps. The front of the label bears the PSO logo, the product name, SKU 7023 and UPC 078345004533 for the sodium hydroxide and SKU 7132 and UPC 078345004625 for the potassium hydroxide.

CPSCMay 20, 2021Nationwide• Chemical Technologies International Inc., dba Pro Supply Outlet, of Rancho Cordova, Calif.

Arrow International Inc: Arrow Temporary Pacing Catheter/Introducer Kit 6Fr. pacin...

Marketed without a 510K

FDAMay 19, 2021Nationwide• Arrow International Inc

Arrow International Inc: Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr...

Marketed without a 510K

FDAMay 19, 2021Nationwide• Arrow International Inc

2018 INTERNATIONAL DURASTAR Recall: FUEL SYSTEM, DIESEL:FUEL INJECTION SYSTEM:FUEL RAIL

Fire/Burn Risk

Navistar, Inc. (Navistar) is recalling certain 2018-2019 International WorkStar, International DuraStar, 2019-2021 International HV, International MV, and IC Bus RE Commercial Bus vehicles. The sealing washer may not seat correctly in the pilot bore holes, allowing the high pressure fuel rail assembly to leak.

NHTSAMay 19, 2021Nationwide• INTERNATIONAL

Arrow International Inc: Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm, Pr...

Marketed without a 510K

FDAMay 19, 2021Nationwide• Arrow International Inc

2019 INTERNATIONAL LT Recall: ENGINE

Navistar, Inc. (Navistar) is recalling certain 2019-2021 International LT and RH trucks. The wrist pin may crack and cause connecting rod failure.

NHTSAApr 22, 2021Nationwide• INTERNATIONAL

Korean Seaweed Snack (JFC International) - Incorrect Packaging (2021)

Wasabi Flavor Seaweed snack is incorrectly packaged in Original Seaweed Flavor package which does not declare FD&C Yellow 5 and FD&C Blue No 1.

Class IIModerate

FDAApr 8, 2021AZ, AR, CA +11 more• J F C International Inc

Deep Blue Essential Oils (doTERRA) – Safety Concerns (2021)

This recall involves doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerball applicator and black cap. The product name, volume amount, SKU, and doTERRA logo are printed on the product labels. The following lot number can be found on the bottom of the bottle: Name Size Lot Number SKU Deep Blue 10 ml 183055, 183232, 190882, 191362, 191484, 192563, 192694, 200853, 202203, 202412, 201622, 202262 60200144 PastTense 10 ml 182621, 190072, 190452, 190512, 190573, 190642, 190662, 190702, 190801, 190921, 191232, 191404, 193451, 200242, 200422, 200932, 201292, 201351, 201392, 201401, 201471, 201481, 201493, 201541, 201551, 201571, 201603, 201673, 201744, 201754, 201822, 201971, 202043 31350001 Deep Blue Touch 10 ml 183094, 190802, 192314, 192666, 193222, 201141, 201923 60200145

CPSCApr 1, 2021Nationwide• doTERRA International LLC, of Pleasant Grove, Utah

2021 INTERNATIONAL RH Recall: PARKING BRAKE

Navistar, Inc. (Navistar) is recalling certain 2021 International LT and International RH vehicles. The spring inside the spring brake chamber may allow the pressure plate to shift and wear a hole through the diaphragm.

NHTSAApr 1, 2021Nationwide• INTERNATIONAL

2021 INTERNATIONAL RH Recall: SERVICE BRAKES, AIR

Navistar, Inc. (Navistar) is recalling certain 2021 International LT, RH, MV, and HV vehicles equipped with Bendix pressure switches. A retainer was not properly seated in the SC-3 single check valve and may not provide source air isolation when pressure is applied. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."

NHTSAApr 1, 2021Nationwide• INTERNATIONAL

Anand Far Far (Babco) – Undeclared Yellow #6 (2021)

Undeclared Allergen

The product was found to contain undeclared yellow# 6, verified via private lab analysis.

Class IIModerate

FDAMar 18, 2021AZ, CA, WA• Babco Foods International, LLC

Arrow International Inc: Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 c...

Difficulty inserting the biopsy ejector rod into the bone lesion biopsy cannula, preventing the biopsy sample from being collected. Use of a defective device is likely to require immediate repeat biopsy, leading to a prolonged procedure

FDAMar 8, 2021Nationwide• Arrow International Inc