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Physician Preferred Medical, LLC

Physician Preferred Medical, LLC Recalls

All product recalls associated with Physician Preferred Medical, LLC.

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

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 12801–12820 of 17593 recalls

Epel Estradiol Pellet (Physician Preferred) – non-sterile (2014)

Non-Sterility: The recalled lot failed sterility testing.

Class IHigh

FDAJul 24, 2014AZ, KS• Physician Preferred Medical, LLC

PosiFlush SF Saline Syringe (Becton Dickinson) – Open Seal Risk (2014)

BD received some reports of open seals found on the BD Posiflush SF Flush Syringe 10 mL (Ref #306553).

Class IIModerate

FDAJul 22, 2014Nationwide• Becton Dickinson & Company

Zenith Slide W-I-D-E Bed (GF Health) – Deck Elevation Problem (2014)

The bed head deck may fail to elevate as expected during normal operation. When the non-operation occurs, the head deck remains in the lowered horizontal / flat position and will no longer function as intended.

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Class II

Moderate

FDAJul 21, 2014Nationwide• GF Health Products, Inc./d.b.a.Basic American Metal Products

Guardian Monitor (Medtronic) – Water Resistance Risk (2014)

Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a manufacturing issue that has the potential to compromise the water resistance of the affected Guardian monitors.

Class IIModerate

FDAJul 21, 2014Nationwide• Medtronic MiniMed Inc.

Transpac IT Kit (ICU Medical) – Connection Crack Risk (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Transpac IV Trifurcated Monitoring Kit w/84" Safeset Rese... (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Yellow Peaches (Wawona) – Potential Contamination (2014)

Listeria

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.

Class IHigh

FDAJul 18, 2014Nationwide• Wawona Packing Company

Yellow Nectarines (Wawona) – Potential Contamination (2014)

Listeria

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.

Class IHigh

FDAJul 18, 2014Nationwide• Wawona Packing Company

White Nectarines (Wawona) – Potential Contamination (2014)

Listeria

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.

Class IHigh

FDAJul 18, 2014Nationwide• Wawona Packing Company

White Peaches (Wawona) – Potential Contamination (2014)

Listeria

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.

Class IHigh

FDAJul 18, 2014Nationwide• Wawona Packing Company

Plums (Wawona) – Potential Contamination (2014)

Listeria

Certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 2 and July 12, 2014 may be contaminated with Listeria monocytogenes.

Class IHigh

FDAJul 18, 2014Nationwide• Wawona Packing Company

Transpac IT Reservoir (ICU Medical) – Connection Crack Risk (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Single Line Transpac IV Monitoring Kit w/ (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Single Transpac IT Monitoring Kit w/ (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Transpac IT w/ (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

BD Multi Check CD4 Low Control Catalog No. 340916 is int... (BD Biosciences, Systems & Reagents) – the outer box label contains the inco... (2014)

The outer box label contains the incorrect distribution date: Box states 2017-09-02 ; should be 2014-09-02

Class IIILow

FDAJul 18, 2014CA, GA, IN +6 more• BD Biosciences, Systems & Reagents

Trifurcated Transpac IV Monitoring Kit w/Safeset Reservoir (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Arterial Transpac IT Monitoring Kit w/Safeset Reservoir (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.

Tetrahydrozoline Hydrochloride (Spectrum) – CGMP deviation (2014)

CGMP Deviations; Stored/dispensed in a non-GMP compliant warehouse at S.I.M.S., Italy.

Class IIModerate

FDAJul 18, 2014CA• Spectrum Laboratory Products

Arterial Safeset Transpac IT w/ (ICU Medical, Inc.) – icu has become aware of an issue with... (2014)

ICU has become aware of an issue with a component where the connection on an arterial monitoring kit may crack and cause a fluid leak.

Class IIModerate

FDAJul 18, 2014OR• ICU Medical, Inc.