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Bellingham Pasta Co

Bellingham Pasta Co Recalls

All product recalls associated with Bellingham Pasta Co.

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Recall Summary

Total Recalls

1000

Past Year

566

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 1221–1240 of 7756 recalls

Roasted Red Pepper Linguine (Bellingham Pasta) - undeclared wheat (2023)

Pasta label declares semolina flour but does not declare wheat.

Class IIModerate

FDAJul 3, 2023IN, WA• Bellingham Pasta Co

Semolina Pappardelle (Bellingham Pasta Co) – Undeclared Wheat (2023)

Pasta label declares semolina flour but does not declare wheat.

Class IIModerate

FDAJul 3, 2023IN, WA• Bellingham Pasta Co

Semolina Sheets (Bellingham Pasta Co) – Undeclared Wheat (2023)

Pasta label declares semolina flour but does not declare wheat.

Class IIModerate

FDA

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Page 62 of 388Next

Jul 3, 2023

IN, WA

• Bellingham Pasta Co

Semolina Bucatini (Bellingham Pasta Co) – Undeclared Wheat (2023)

Pasta label declares semolina flour but does not declare wheat.

Class IIModerate

FDAJul 3, 2023IN, WA• Bellingham Pasta Co

Semolina Lemon Black Pepper Linguine (Bellingham Pasta Co) – Undeclared Wheat (2023)

Pasta label declares semolina flour but does not declare wheat.

Class IIModerate

FDAJul 3, 2023IN, WA• Bellingham Pasta Co

Leather Woven Chairs (H-E-B) – Fall Hazard (2023)

This recall involves H-E-B's Haven & Key Leather Woven Chairs, also referred as "Lovina Chairs." The recalled chairs were sold in black or brown. UPC codes are 4122089244 (black) and 4122091920 (brown). The UPC codes are displayed on the hangtag.

CPSCJun 29, 2023Nationwide• UD Surya Abadi Furniture, of Indonesia

Safe Tussin DM Cough Syrup (Kramer) – Non-Food Grade Lubricant (2023)

CGMP Deviations: use of non-food grade lubricant in mixing vessel.

Class IIModerate

FDAJun 23, 2023Nationwide• Kramer Laboratories, Inc.

Safe Tussin PM Cough Syrup (Kramer) – Non-Food Grade Lubricant (2023)

CGMP Deviations: use of non-food grade lubricant in mixing vessel.

Class IIModerate

FDAJun 23, 2023Nationwide• Kramer Laboratories, Inc.

Apple Cider (CN Smith) – Patulin Contamination (2023)

Product contains high levels of patulin (above 50ppb).

Class IIModerate

FDAJun 23, 2023CT, MA, NH +1 more• Bevovations, LLC

Diclofenac Sodium Topical Solution (Alembic) – Delivery System Defect (2023)

Defective Delivery System

Class IIModerate

FDAJun 22, 2023Nationwide• ALEMBIC PHARMACEUTICALS, INC.

Liquid Urine Control (Randox) – Test Result Variation (2023)

(1) There is vial to vial variation resulting in some vials recovering positive for hCG, which should be negative and (2) high and outside range for cortisol. (3) There has been a transcription error for Creatinine in the Instructions For Use (IFU). The target and ranges for Creatinine for the Roche Creatinine Plus method have been listed incorrectly. These failures cause a delay in patient results for the above mentioned analytes.

FDAJun 21, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Level-1 Protein (1st Phorm) – Bacterial contamination (2023)

Product may contain Staphylococcus aureus.

Class IIModerate

FDAJun 21, 2023MO• International Food Companies DBA International Food Products

Tizanidine 4mg Tablets (Dr Reddy's) – Dissolution Specification (2023)

Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.

Class IIModerate

FDAJun 21, 2023Nationwide• Dr Reddy's Laboratories Limited

Ringed DxI Reaction Vessels (Beckman Coulter) – System Compatibility (2023)

Beckman Coulter, Inc. is recalling Ringed DxI Reaction Vessels (RVs) as part of Unicel DxI Immunoassay System (600, 800 series). The reason for the recall is that the firm has identified 3 lots of RVs that failed an internally used service test to evaluate washing efficiency. Increased relative light units (RLU) suspected to be caused by the resulting rough interior surface may lead to artificially falsely elevated results for susceptible tests, in particular, sandwich assays including, but not limited to, hsTnI, Hybritech p2PSA, IPTH/IPTH IO.

FDAJun 20, 2023Nationwide• Beckman Coulter, Inc.

GEM Flow Coupler Monitor (Baxter) – Display Channel Error (2023)

An issue was identified where the LCD monitor display may not indicate the correct active channel. The issue occurs when the monitor is turned on using battery power, and channel B was selected as the last active channel prior to powering down.

FDAJun 19, 2023Nationwide• Baxter Healthcare Corporation

Spectrum IQ Infusion System (Baxter) – Device Correction (2023)

A medical device correction is being issued for SIGMA Spectrum Infusion System (V8 Platform) and Spectrum IQ Infusion System with Dose IQ Safety Software infusion pumps due to an increase in reported false upstream occlusion alarms following upgrades to software versions v8.01.01 and v9.02.01.

FDAJun 15, 2023Nationwide• Baxter Healthcare Corporation

SIGMA Spectrum Infusion Pump (Baxter) – Device Correction (2023)

FDAJun 15, 2023Nationwide• Baxter Healthcare Corporation

RX Series Urea Enzymatic Assay (Randox) – Carryover Bias (2023)

Carryover from the Direct LDL-cholesterol assay on the Rx instruments may result in a negative bias, up to -11%, in quality control and patient samples, in urea assays results if the urea assay is run immediately after the Direct LDL-cholesterol assay. This may lead to a delay in reporting results or in falsely decreased urea test results.

FDAJun 13, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Sterile Ultrasound Gel (Turkuaz) – Sterility Concern (2023)

Sterility of Ultrasound gel can not be guaranteed.

FDAJun 9, 2023IL• Turkuaz Saglik Hizmetleri Medikal Temizlik Kim. Ur. San. ve Tic. A.S. Akcaburgaz Mahallesi Muhsin Yazicioglu Caddesi No:45/5 Esenyurt Turkey

Kate and Laurel Mirrors (Uniek) – laceration hazard (2023)

Laceration Risk

This recall involves Kate and Laurel-branded Astora Capsule and Valenti Short Wood Arch mirrors. The oval-shaped Astora mirrors measure about 16 inches high and 36 inches wide. They have a wooden frame and a bottom shelf in walnut or natural finishes. The arch-shaped Valenti mirrors measure about 24 inches high and 32 inches wide and were sold in a walnut finish.

CPSCJun 8, 2023Nationwide• Ningbo Zhenhai Tianen Photo Frame Manufacturing Co. Ltd., of China