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HS Baking Enterprises LLC DBA Darlington Manufacturing

HS Baking Enterprises LLC DBA Darlington Manufacturing Recalls

All product recalls associated with HS Baking Enterprises LLC DBA Darlington Manufacturing.

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

Most Recent

Dec 2025

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 3561–3580 of 10937 recalls

Darlington Soft Baked Cookies – Undeclared Milk (2020)

An internal quality review found that an ingredient contained a milk derivative, but milk was not declared on the label.

Class IIILow

FDADec 4, 2020IL, IN, NY• HS Baking Enterprises LLC DBA Darlington Manufacturing

Honda Pioneer ROVs – Crash and Injury Risk (2020)

This recall involves Model Year 2017-2019 & certain 2020 Honda Pioneer 700 and 2016-2019 & certain 2020 Pioneer 1000 Side-by-Side vehicles equipped with Electric Power Steering (EPS). The recalled vehicles were sold in various colors including: Red, blue, green, gray and yellow. The name "HONDA" is on the front, sides and the rear of the vehicle. The model name Pioneer 700 or Pioneer 1000 is printed on a label located on both sides of the vehicle. The serial number (VIN #) is stamped in the frame at the left rear, below the tilt-up bed/seat. MY Model VIN Start VIN End 2017 Pioneer 700 - 2 Passenger SXS700M2* 1HFVE02**H4300001 1HFVE02**H4303722 2017 Pioneer 700 - 4 Passenger SXS700M4* 1HFVE02**H4300001 1HFVE02**H4350720 2018 Pioneer 700 - 2 Passenger SXS700M2* 1HFVE02**J4400001 1HFVE02**J4402760 2018 Pioneer 700 - 4 Passenger SXS700M4* 1HFVE02**J4400001 1HFVE02**J4451320 2019 Pioneer 700 - 2 Passenger SXS700M2* 1HFVE02**K4500001 1HFVE02**K4502100 2019 Pioneer 700 - 4 Passenger SXS700M4* 1HFVE02**K4500001 1HFVE02**K4550600 2020 Pioneer 700 - 2 Passenger SXS700M2* 1HFVE02**L4600001 1HFVE02**L4601500 2020 Pioneer 700 - 4 Passenger SXS700M4* 1HFVE02**L4600001 1HFVE02**L4650780 2016 Pioneer 1000 - 3 Passenger SXS1000M3* 1HFVE04**G4000001 1HFVE04**G4008403 2016 Pioneer 1000 - 5 Passenger SXS1000M5* 1HFVE04**G4000001 1HFVE04**G4010507 2017 Pioneer 1000 - 3 Passenger SXS1000M3* 1HFVE04**H4100001 1HFVE04**H4102101 2017 Pioneer 1000 - 5 Passenger SXS1000M5* 1HFVE04**H4100001 1HFVE04**H4103000 2018 Pioneer 1000 - 3 Passenger SXS1000M3* 1HFVE04**J4200001 1HFVE04**J4205460 2018 Pioneer 1000 - 5 Passenger SXS1000M5* 1HFVE04**J4200001 1HFVE04**J4210320 2019 Pioneer 1000 - 3 Passenger SXS1000M3* 1HFVE04**K4300001 1HFVE04**K4301920 2019 Pioneer 1000 - 5 Passenger SXS1000M5* 1HFVE04**K4300001 1HFVE04**K4302460 2020 Pioneer 1000 - 3 Passenger SXS1000M3* 1HFVE04**L4400001 1HFVE04**L4403180 2020 Pioneer 1000 - 5 Passenger SXS1000M5* 1HFVE04**L4400001 1HFVE04**L4404620

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High

CPSCDec 3, 2020Nationwide• American Honda Motor Co., Inc., of Torrance, Calif.

ICU Medical Extension Set (ICU Medical) – Filter Assembly Problem (2020)

Due to the incorrect filter assembly.

Moderate

FDADec 2, 2020Nationwide• ICU Medical, Inc.

ICU Medical Smallbore Set (ICU Medical) – Filter Assembly Problem (2020)

Due to the incorrect filter assembly.

Moderate

FDADec 2, 2020Nationwide• ICU Medical, Inc.

ICU Medical Extension Set (ICU Medical) – Filter Assembly Problem (2020)

Due to the incorrect filter assembly.

Moderate

FDADec 2, 2020Nationwide• ICU Medical, Inc.

ICU Medical Smallbore Set (ICU Medical) – Filter Assembly Problem (2020)

Due to the incorrect filter assembly.

Moderate

FDADec 2, 2020Nationwide• ICU Medical, Inc.

Pristine Hand Sanitizer Gel (GAZA) – cGMP Deviation (2020)

cGMP deviations: Product made at the same facility where product tested was sub-potent.

Class IIModerate

FDADec 1, 2020TX• GAZA PROVEEDORA DE SERVICIOS DE HOSPEDAJE Y ALIMENTACION

Zapien Hand Sanitizer Gel (GAZA) – cGMP Deviation (2020)

cGMP deviations: Product made at the same facility where product tested was sub-potent.

Class IIModerate

FDADec 1, 2020TX• GAZA PROVEEDORA DE SERVICIOS DE HOSPEDAJE Y ALIMENTACION

CM Injectate Kit (Lidco) – Incorrect Expiration Date (2020)

The expiration date on labeling is incorrect.

Low

FDANov 19, 2020Nationwide• Lidco Ltd 16 Orsman Road London United Kingdom

Percept PC Neurostimulator (Medtronic) – Connection Failure (2020)

A software anomaly in the A620 Patient Programmer application was identified that results in failure to connect with the Percept PC device.

Moderate

FDANov 19, 2020Nationwide• Medtronic Neuromodulation

RZR Off-Highway Vehicles (Polaris) – injury hazard (2020)

This recall involves Model Year 2020 RZR PRO XP and RZR PRO XP 4 and Model Year 2021 RZR PRO XP, RZR PRO XP 4, RZR Turbo S, RZR Turbo S 4, RZR XP Turbo and RZR XP 4 Turbo recreational off-highway vehicles. The two or four-seat vehicles were sold in the following colors: Black, blue, gray, lime (green), sand (light brown), orange, red, titanium (silver) and white. POLARIS is stamped on the front grille and POLARIS and RZR are printed on the sides of the vehicles. Model Year Model Name 2020 RZR PRO XP 2020 RZR PRO XP 4 2021 RZR PRO XP 2021 RZR PRO XP 4 2021 RZR Turbo S 2021 RZR Turbo S 4 2021 RZR XP Turbo 2021 RZR XP 4 Turbo

Moderate

CPSCNov 19, 2020Nationwide• Polaris Inc., of Medina, Minn.

BD PrecisionGlide Needle (BD) – Blood Contamination (2020)

BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 9128897. The possibility of infection may be present if the blood is not noticed prior to use by the clinician.

Moderate

FDANov 18, 2020Nationwide• Becton Dickinson & Company

Trinias X-Ray System (Shimadzu) – Ceiling Arm Control Issue (2020)

The firm has identified a problem with the control software for the celling arm of the X-Ray System . This software issue could cause the ceiling arm of the device to move after the operator has released the movement lever. This could result in possible collision or harm to the patient or system operator.

Moderate

FDANov 18, 2020Nationwide• Shimadzu Medical Systems

MH-200S X-Ray System (Shimadzu) – Ceiling Arm Control Issue (2020)

Moderate

FDANov 18, 2020Nationwide• Shimadzu Medical Systems

Bransist Safire X-Ray System (Shimadzu) – Ceiling Arm Control Issue (2020)

Moderate

FDANov 18, 2020Nationwide• Shimadzu Medical Systems

Tempus LS Defibrillator (Remote Diagnostic) – Software Error (2020)

A software error was detected within software version 1.3.4 for the Tempus LS device. When exiting pacer back into manual mode the pacer pulse wave may put the ECG calibration out of calibration. This software error may result in a delay in therapy, as the clinician is not provided an ECG waveform on which a shockable rhythm decision can be made. The device is still able to deliver a manual defibrillation shock.

Moderate

FDANov 17, 2020Nationwide• Remote Diagnostic Technologies Ltd. PAVILION C2, ASHWOOD PARK ASHWOOD WAY Basingstoke United Kingdom

Sicilian Seasoning (Victoria Gourmet) – undeclared sesame (2020)

Undeclared Allergen

Product contains undeclared sesame.

Class IIModerate

FDANov 17, 2020Nationwide• Victoria Gourmet, Inc.

Cobalt HF CRT-D Implant (Medtronic) – Device Performance (2020)

Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.

High

FDANov 15, 2020GA, NJ, PA• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Cobalt DR MRI Implant (Medtronic) – Device Performance (2020)

Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.

High

FDANov 15, 2020GA, NJ, PA• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Cobalt HF Quad CRT-D (Medtronic) – Device Performance (2020)

Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.

Moderate

FDANov 15, 2020GA, NJ, PA• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)