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The Procter & Gamble Company

The Procter & Gamble Company Recalls

All product recalls associated with The Procter & Gamble Company.

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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 6621–6640 of 25000 recalls

Secret Powder Fresh (P&G) – benzene contamination (2021)

CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene

Class IIModerate

FDANov 23, 2021Nationwide• The Procter & Gamble Company

Old Spice Pure Sport (P&G) – manufacturing deviation (2021)

CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene

Class IIModerate

FDANov 23, 2021Nationwide• The Procter & Gamble Company

Old Spice Pure Sport Gift Set (Procter & Gamble) – Facility Contamination (2021)

CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene

1...330 331332333 334...1250

Page 332 of 1250Next

Class II

Moderate

FDANov 23, 2021Nationwide• The Procter & Gamble Company

Old Spice Pure Sport Plus (P&G) – benzene contamination (2021)

CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene

Class IIModerate

FDANov 23, 2021Nationwide• The Procter & Gamble Company

Avanos Medical, Inc.: BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel ...

Product was distributed with incorrect expiration date.

FDANov 22, 2021Nationwide• Avanos Medical, Inc.

Avanos Medical, Inc.: BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbo...

Product was distributed with incorrect expiration date.

FDANov 22, 2021Nationwide• Avanos Medical, Inc.

Cardiovascular Systems Inc: WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and F...

Under certain circumstances, the WIRION filter assembly may become difficult to withdraw. Under such circumstances, alternative means may be necessary for withdrawal and the device may be prone to tearing or separating which may result in a risk for embolization.

FDANov 22, 2021Nationwide• Cardiovascular Systems Inc

Avanos Medical, Inc.: BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Ca...

Product was distributed with incorrect expiration date.

FDANov 22, 2021Nationwide• Avanos Medical, Inc.

Organic Blue Corn Tortilla Chips (Trader Joe's) – undeclared milk (2021)

Undeclared Allergen

Popcorn containing butter (milk) was found co-mingled with Trader Joe's Organic Blue Corn Tortilla Chips - undeclared milk allergen.

Class IIModerate

FDANov 22, 2021DE, IL, IN +15 more• Trader Joes Company

DiaSorin Molecular LLC: Simplexa Direct Amplification Disc Kit, Product Kit Code ...

A subset of affected discs are at risk of leakage when it is used more than one time with Simplexa COVID-19 Direct and/or Simplexa Flu A/B & RSV Direct Gen II. Leakage from a well that had a positive sample may cause further cross-contamination in areas of the lab if not properly cleaned.

FDANov 19, 2021AZ, CA, CO +38 more• DiaSorin Molecular LLC

Medtronic Sofamor Danek USA Inc: Distractor Rack, REF 5598007, which may be packaged in Mo...

Two lots of the 5598007 Distractor Rack which were not manufactured to specification. The crest width of the gear is too wide and may cause difficulty or the inability to operate the Distractor.

FDANov 19, 2021CT, IN, NE• Medtronic Sofamor Danek USA Inc

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): Instructions for Use for all model numbers of the Medtron...

There have been reports of stent migration.

FDANov 19, 2021Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

KEY SAFETY SYSTEMS CURTAIN AIRBAG INFLATOR Equipment Recall: AIR BAGS:SIDE/WINDOW:CURTAIN

Key Safety Systems, Inc. (DBA Joyson) is recalling certain Curtain Air Bag Inflators, model HPH-A, and part numbers 2546178-AD, 2546179-AD, 2546180-AD, and 2546219-AE. The air bag inflators may have been manufactured with the incorrect amount of compressed gas, which could result in an improper air bag deployment.

NHTSANov 19, 2021Nationwide• KEY SAFETY SYSTEMS

Philips North America Llc: Philips Allura Xper FD series with Software Version Numbe...

Set screws securing the two gliding rods of the Extra Monitors (called 7th and 8th monitor) mounted on the Monitor Ceiling Suspension (MCS) can come loose, the Extra monitors might disengage from the Mounting Ceiling Suspension structure and fall down, may lead to patient, user or service engineer harm that may require medical intervention.

FDANov 19, 2021Nationwide• Philips North America Llc

Hand Sanitizer (American Screening) – Improper Packaging (2021)

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

Class IHigh

FDANov 19, 2021Nationwide• American Screening LLC

Hydrocodone Bitartrate Acetaminophen Tablets (Ascent Pharmaceuticals) – Product Mix-up (2021)

Product Mix-up

Class IIModerate

FDANov 19, 2021Nationwide• Ascent Pharmaceuticals, Inc.

Tydemy (Lupin Pharmaceuticals) – Subpotent Drug (2021)

Subpotent Drug

Class IIILow

FDANov 19, 2021Nationwide• Lupin Pharmaceuticals Inc.

Pioneer and Talon ROVs (Honda) – crash and injury hazard (2021)

This recall involves the 2021 Honda Pioneer 700, Pioneer 1000, and Talon 1000 recreational off-highway vehicles (ROVs) equipped with electric power steering. The vehicles come in various colors including red, blue, green, gray, and yellow. "HONDA" is printed on the front, sides, and the rear of each vehicle. The name of the vehicle is printed on a label located on both sides of the vehicle. The VIN number is stamped in the frame at the left rear below the tilt-up bed/seat on the Pioneer 700 and Pioneer 1000. The VIN number is stamped in the frame on the left side under the left front fender for the Talon 1000. The VIN number range of affected vehicles for the Pioneer 700 is 1HFVE02**M4700031-M4700694, for the Pioneer 1000 is 1HFVE04**M4500061-M4502219, and for the Talon 1000 is 1HFVE05**M4200001-M4201598.

CPSCNov 18, 2021Nationwide• American Honda Motor Co. Inc., of Torrance, California

Evaporator Coil Drain Pans (Goodman) – installation risk (2021)

Fire/Burn Risk

This recall involves evaporator coil drain pans paired with residential condensing gas furnaces that are installed in a vertical, or "up-flow," configuration. Furnaces in this configuration that were installed or repaired with a new evaporator coil drain pan between January 2019 and November 2021 are affected by this recall. Only evaporator drain pans with serial numbers with prefixes ranging from 1901 through 2101 are covered by this recall. The evaporator coil, which sits atop the vertically installed furnace, will either be cased or uncased. The evaporator coil's serial number is displayed on a label attached to both cased and uncased models. For cased evaporator coils, the serial number is on the label attached to the coil case. For uncased units, the serial number is on a label attached to the front of the coil. It may be necessary to determine the brand and model number of your existing furnace in order to provide the correct repair kit. In most instances, the furnace brand and model number can be found on your furnace on the "Energy Guide" label. For all other instances, please refer to the instructions on Goodman's model verification tool at: www.recallrtr.com/drainpan The model number of the outdoor condenser your furnace is paired with may also be required. The model number can be found on a label attached to the outdoor condenser.

CPSCNov 18, 2021Nationwide• Goodman Manufacturing Company L.P., of Houston, Texas (evaporator coils)

Roche Molecular Systems, Inc.: cobas LiatSystem, respiratory virus panel nucleic acid as...

Roche has identified a small number of cobas Liat analyzer units that have consistently high noise levels (background signal) originating from the amber detector (used for Influenza B detection). This noise increases the probability of false positive Influenza B results.

FDANov 16, 2021Nationwide• Roche Molecular Systems, Inc.