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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

567

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 2581–2600 of 7756 recalls

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 Large (Professional Disposables) – Subpotent Specification (2021)

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 II

1...128 129130131 132...388

Page 130 of 388Next

Moderate

FDAJul 23, 2021Nationwide• Professional Disposables International, Inc

Baxter Healthcare Corporation: Baxter prismaflex, HF 1000 PAES membrane, REF 107140 Us...

Products labeled as sterile were distributed, but may not have been sterilized. Baxter confirmed Steril Milano observed nonconformances that were not reported to Baxter Data was manipulated to appear to be conforming

FDAJul 22, 2021Nationwide• Baxter Healthcare Corporation

Baxter Healthcare Corporation: Baxter PrismaFlex, REF numbers: a) 106696 (M 60 SET) b)...

Products labeled as sterile were distributed, but may not have been sterilized. " Baxter confirmed Steril Milano observed nonconformances that were not reported to Baxter. Data was manipulated to appear to be conforming

FDAJul 22, 2021Nationwide• Baxter Healthcare Corporation

Beckman Coulter Inc.: DxA 5000 (DxA Automation System, DxA 5000 fit), "For in V...

There is a potential that sample carriers (w or w/o samples) within automated sampling system may transport samples to the outer lane which does not contain a physical barrier to restrain samples. Samples are dropped when they reach the end of the outer lane which could result in Delay in providing patient with appropriate medical treatment. New sample needs to be drawn. Substantial discharge of biohazards material - Infection with a human transmissible blood-borne or animal pathogen which could result in Infection with a human transmissible blood-borne pathogen (e.g. infectious HBV, HCV, HIV).

FDAJul 21, 2021Nationwide• Beckman Coulter Inc.

Belmont Instrument Corporation: CritiCool, thermoregulation device

Premature pump failure may lead to the device displaying a HALT 4 error, from which the device cannot recover even after device reboot. The issue may potentially lead to delayed treatment and a failure to deliver the prescribed thermoregulation therapy. To date, the firm has received one report of death potentially related to this issue.

FDAJul 20, 2021Nationwide• Belmont Instrument Corporation

BioFire Diagnostics, LLC: FilmArray Blood Culture Identification (BCID) Panel Prod...

Due to product complaints received for false negative results (dropouts) with blood culture identification panel potential caused by a pouch manufacturing error.

FDAJul 20, 2021Nationwide• BioFire Diagnostics, LLC

Tizanidine HCl Tablets 4mg (Dr. Reddy's) – Tablet Specification Failure (2021)

Failed Tablet/Capsule Specification: Some tablets are shaved

Class IIModerate

FDAJul 19, 2021Nationwide• Dr. Reddy's Laboratories, Inc.

Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland: RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set, ...

The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.

FDAJul 16, 2021Nationwide• Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland

Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland: RUSCH Endotracheal Tube oral/nasal Magill, High Volume, L...

The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.

FDAJul 16, 2021Nationwide• Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland

Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland: RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, ...

The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.

FDAJul 16, 2021Nationwide• Teleflex Medical Europe Ltd Ida Business Park Athlone Ireland

Beckman Coulter Inc.: Normand Remisol Advance Data Manager, REF: C69412, C69413...

There is a potential that the data management system may add additional cells to the patient request which could lead to erroneous patient result.

FDAJul 15, 2021Nationwide• Beckman Coulter Inc.

Abbott Laboratories, Inc: Alinity s System REF 06P16-01. An automated immunoassay...

A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators.

FDAJul 12, 2021Nationwide• Abbott Laboratories, Inc

PROCEPT BIOROBOTICS CORPORATION: AQUABEAM Handpiece, REF: HP2000, a sterile single-use com...

Scope tube tip may detach from the telescoping tube, which is attached to a single-use handpiece, a component of an aquablation robotic system. Both tip detachment and entire tip separation form the handpiece may lead to procedural delay for handpiece exchange. Tip detachment can be seen cystoscopically and tip separation from the handpiece may necessitate tip removal from the bladder or prostate.

FDAJul 9, 2021Nationwide• PROCEPT BIOROBOTICS CORPORATION

Copan Italia Via Francesco Perotti 10 Brescia Italy: COPAN FLOQSwabs, STERILE.EO, for drawing clinical sample...

A sterility assurance level of 10-6 cannot be guaranteed due to intentional fraud and data integrity issues at the contract sterilizer, Steril Milano.

FDAJul 9, 2021Nationwide• Copan Italia Via Francesco Perotti 10 Brescia Italy

Baxter Healthcare Corporation: Dose IQ Safety Software used with Spectrum IQ Infusion Pump

Software issue: The defect creates a mismatch between linked drug identifiers (IDs) in the Dose IQ user interface (UI) and the binary drug library (BDL) loaded onto the Spectrum IQ pump.

FDAJul 7, 2021Nationwide• Baxter Healthcare Corporation

Laboratoires Bodycad, Inc.: Torque Limiting Adaptor, AO Connect, 4 N-m, part #027-203...

There is a risk of breakage of the torque limiting adaptor if used counterclockwise and it must not be used with a power tool due to no test data validating this use.

FDAJul 2, 2021CO, MI, NY• Laboratoires Bodycad, Inc.

2020 BRAXTON CREEK LX Recall: EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS

Fire/Burn Risk

Braxton Creek RV (Braxton) is recalling certain 2020-2021 LX and BX travel trailers, equipped with Dometic R1731, R2131, and S31 3-burner cooking stoves. The saddle valve securing bolt may be overtightened, possibly damaging the o-ring seal and causing a continuous gas leak.

NHTSAJul 2, 2021Nationwide• BRAXTON CREEK

Liquid Nicotine (TBD Liquids) – Packaging Violation (2021)

This recall involves "The Best Damn Liquids" branded liquid nicotine products in all flavors packaged in clear plastic bottles in 120 mL and 240 mL sizes with a continuously threaded closure.

CPSCJul 1, 2021Nationwide• TBD Liquids LLC, of Santa Rosa, Calif.