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Port City Bakery, Inc

Port City Bakery, Inc Recalls

All product recalls associated with Port City Bakery, Inc.

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Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

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 3321–3340 of 11124 recalls

Ultimo Par Baked Pizza Crust – Glass Contamination (2020)

Frozen pizza crust may contain foreign material (glass).

Class IIModerate

FDADec 29, 2020IL, WI• Port City Bakery, Inc

Port City Par Baked Pizza Crust – Glass Contamination (2020)

Frozen pizza crust may contain foreign material (glass).

Class IIModerate

FDADec 29, 2020IL, WI• Port City Bakery, Inc

Par Baked Pizza Crust (Port City Bakery) – Glass Contamination (2020)

Frozen pizza crust may contain foreign material (glass).

Class IIModerate

FDA

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Page 167 of 557Next

Dec 29, 2020

IL, WI

• Port City Bakery, Inc

14" Stuffed Pizza Crust (Port City Bakery) – Glass Contamination (2020)

Frozen pizza crust may contain foreign material (glass).

Class IIModerate

FDADec 29, 2020IL, WI• Port City Bakery, Inc

Levetiracetam Oral Solution (Akorn) – Leaking Bottle (2020)

Defective container: Customer complaints for oral solution leaking from bottles.

Class IIModerate

FDADec 28, 2020Nationwide• Akorn, Inc.

Excedrin Migraine Caplets (GSK) – Packaging Safety (2020)

This recall involves 50, 80, 100, 125, 200, 250 and 300-count bottles of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets. The bottles are plastic with a child-resistant closure. For a full list of the recalled products, visit www.excedrin.com/products/discontinued.

Low

CPSCDec 23, 2020Nationwide• GSK Consumer Healthcare, of Warren, N.J.

Hypodermic Syringe (Becton Dickinson) – Packaging Seal Issue (2020)

The product packaging for the 10 ml eccentric tip syringe may exhibit open seals. An open seal impacts package integrity and potentially compromises sterility of the syringe.

Low

FDADec 23, 2020Nationwide• Becton Dickinson & Company

Hand Sanitizer (Shane Erickson) – Ethanol Deviation (2020)

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Class IIModerate

FDADec 23, 2020Nationwide• Shane Erickson Inc

Hand Sanitizer (Shane Erickson) – Ethanol Deviation (2020)

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Class IIModerate

FDADec 23, 2020Nationwide• Shane Erickson Inc

Hand Sanitizer (Shane Erickson) – Ethanol Deviation (2020)

CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.

Class IIModerate

FDADec 23, 2020Nationwide• Shane Erickson Inc

Aquarius LPH Probe (Cytocell) – Signal Variation Risk (2020)

Users may observe very faint additional locus specific signals at 11q13. There is a low risk of a normal sample being reported as not normal in a resulting laboratory developed test (LDT) that utilizes the LPH511-A CRLF2 Distal Probe Green.

Moderate

FDADec 22, 2020CA, IL, MI +4 more• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

PSG-1100 Sleep System (Nihon Kohden) – Safety Standard Issue (2020)

Medical device non-conformance to electrical safety standard (IEC 60601-1).

Moderate

FDADec 21, 2020Nationwide• Nihon Kohden America Inc

Cougar RV (Keystone) – Electrical System Issue (2020)

Fire/Burn Risk

Keystone RV Company (Keystone) is recalling certain 2021 Cougar 22MLS, 22RBS, 25RDS, 26RBS, 26RKS, 27RES, 29BHS, 30RKD, 31MBS, 32RLI and 34TSB recreational trailers equipped with a Solar Prep or an off-the-grid "OTG" Solar Camping Package. The Solar Prep wiring to the 12VDC breakers located by the battery may not be connected to the protected side of the breaker.

High

NHTSADec 18, 2020Nationwide• KEYSTONE

Benzhydrocodone Tablets (KVK-Tech) – Impurity Issue (2020)

Failed Impurities/Degradation Specifications; out of specification results obtained for N-Oxide impurity during the 12-month long term stability testing for Batch# 15892A

Class IIILow

FDADec 18, 2020Nationwide• KVK-Tech, Inc.

Compact Suction Unit (Laerdal) – Suction Loss Risk (2020)

Component failures may cause the unit to lose all suction. Users will need to obtain alternate suction devices or methods, leading to a delay in treatment and, in worst case scenario, potential suffocation if alternative suction or ventilation method is not administered by the user.

Very High

FDADec 18, 2020Nationwide• Laerdal Medical (Suzhou) Co., Ltd. Science & Technology Ind. Park No.

Beetle Convertible (Volkswagen) – Airbag Deployment Risk (2020)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2012-2014 Volkswagen Beetle and Beetle Convertible vehicles. The driver's side air bag inflator may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, high temperatures, and high temperature cycling.

Very High

NHTSADec 16, 2020Nationwide• VOLKSWAGEN

Western Chief Toddler Boots – Choking Hazard (2020)

Choking Hazard

This recall includes the Western Chief "Abstract Camo," "Alia Silver," and "Sweetheart Navy" Light-Up Rain Boots in sizes 5-12 for toddlers or children. The recalled boots are camouflage, silver glitter, and navy with hearts; include boot handles; and have a light up feature in the heel of the boot. The rivets used to attach the handles are silver-gray in color. "Western Chief" and the model numbers are located on the inside tag of the boot. The recalled model numbers are T24121725P, T24121728P, and T24121729P.

Moderate

CPSCDec 9, 2020Nationwide• Washington Shoe Company, of Kent, Wash.