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Deva Holding AS - Cerkezkoy Subesi

Deva Holding AS - Cerkezkoy Subesi Recalls

All product recalls associated with Deva Holding AS - Cerkezkoy Subesi.

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Recall Summary

Total Recalls

398

Past Year

21

Class I (Serious)

8

Most Recent

Nov 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 241–260 of 398 recalls

Temozolomide Capsules 100mg (Deva Holding) – Cross-Contamination Risk (2019)

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Class IIModerate

FDAJul 16, 2019Nationwide• Deva Holding AS - Cerkezkoy Subesi

Temozolomide Capsules 20mg (Deva Holding) – Cross-Contamination Risk (2019)

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Class IIModerate

FDAJul 16, 2019Nationwide• Deva Holding AS - Cerkezkoy Subesi

Temozolomide Capsules 140mg (Deva Holding) – Cross-Contamination Risk (2019)

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

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Class IIModerate

FDAJul 16, 2019Nationwide• Deva Holding AS - Cerkezkoy Subesi

Temozolomide Capsules 180mg (Deva Holding) – Cross-Contamination Risk (2019)

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Class IIModerate

FDAJul 16, 2019Nationwide• Deva Holding AS - Cerkezkoy Subesi

Temozolomide Capsules 5mg (Deva Holding) – Cross-Contamination Risk (2019)

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Class IIModerate

FDAJul 16, 2019Nationwide• Deva Holding AS - Cerkezkoy Subesi

Temozolomide Capsules 250mg (Deva Holding) – Cross-Contamination Risk (2019)

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Class IIModerate

FDAJul 16, 2019Nationwide• Deva Holding AS - Cerkezkoy Subesi

Stryker GmbH Bohnackerweg 1 Selzach Switzerland: Endotrac EPF/EGR Hook/Triangle Blade Kit, Catalogue Numbe...

The seal integrity of the sterile bag containing the kits may be compromised.

FDAApr 30, 2019Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Stryker GmbH Bohnackerweg 1 Selzach Switzerland: Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2...

The seal integrity of the sterile bag containing the kits may be compromised.

FDAApr 30, 2019Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

Karl Storz Endoscopy: Flexible Intubation Fiberscope, Model # 11301AB1

The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.

FDAApr 24, 2019CA, CO, LA +6 more• Karl Storz Endoscopy

Stove Top Espresso Makers (Bodum) – fire and burn hazard (2019)

This recall involves CHAMBORD® stove top espresso makers in a stainless steel finish. The recall includes 6-cup (12 ounce) espresso makers with SKU number 10617-16. This SKU number appears on the packaging of the product. The word "Bodum" is embossed on the lower half of the product.

CPSCApr 23, 2019Nationwide• Kimcoland (Zhejiang Goldsen) Industry and Trade Co. Ltd., of China

Yemeni Spices Mix (Makzemo) – Lead Contamination (2019)

Product contains high levels of lead.

FDAApr 11, 2019MI, NY• Makzemo LLC

Performance Heated Socks (Mobile Warming) – fire risk (2019)

This recall involves Mobile Warming Performance Heated Socks sold with lithium-ion batteries. Only socks with serial number MW18A04-17-14, MW18A04-17-15, MW18A04-M4-10/W6-11 and MW18A04-M10-14 are included in the recall. These socks are gray and made of a poly-cotton blend in men's and women's size 6-10 and 10-14. The socks heat when the battery is connected and is in the on position. The heating on/off is controlled through the battery switch or the phone app when a phone is paired.

CPSCMar 14, 2019Nationwide• Mi Croteck Gaoke (HK) Limited/Shenzhen FCY Technology Co. Ltd, of China

2019 KZRV SPORTSMEN Recall: EQUIPMENT

KZRV, L.P. (KZRV) is recalling certain 2019 RV Sonic Lite, Sportsmen Classic and Escape recreational trailers equipped with a Capital liquid propane (LP) Gas Drop-in 2 Burner cooktop. The cooktop's flame may become inverted when the furnace is running.

NHTSAMar 4, 2019Nationwide• KZRV

Kingpin Ski Bindings (Marker) – Fall Safety Risk (2018)

This recall involve s 2017-2018 Kingpin models 10 and 13 ski binding, with a black body and gold or copper accent coloring. The bindings are used with alpine touring ski boots with metal pintech inserts in the toe of each boot. The recalled toe units have heel units with serial numbers on the back in the following ranges: Kingpin 10 (337804 - 418632) and Kingpin 13 (337798 - 411728). Model Number Product Name Accent Color 7733R1MA KINGPIN 10; 75 - 100 mm gold 7733R1MB KINGPIN 10; 100 - 125 mm gold 7933R1MA KINGPIN 13; 75 - 100 mm gold 7734R1MA KINGPIN 10 Demo; 75 - 100 mm gold 7934R1MB KINGPIN 13 Demo; 100 - 125 mm gold 7933R1MB KINGPIN 13; 100 - 125 mm gold 7733S1MA KINGPIN 10; 75 - 100 mm copper 7733S1MB KINGPIN 10; 100 - 125 mm copper 7933S1MA KINGPIN 13; 75 - 100 mm copper 7933S1MB KINGPIN 13; 100 - 125 mm copper 7734S1MA KINGPIN 10 Demo; 75 - 100 mm copper 7934S1MB KINGPIN 13 Demo; 100 - 125 mm copper

CPSCOct 9, 2018Nationwide• Marker CZ, of Czech Republic

Pepperoni Pizza Kit (K.B. Pizza) – Unknown safety issue (2018)

K.B. Pizza, Inc. has initiated a recall of Son of Italy Cheese Kit, Son of Italy Pepperoni Kit, 39 oz./2 pizzas per kit, Vacuum packed, 6 kits per case. Use by date of 12-5-18 on each kit and case, because the pizza kits were left at room temperature for 24 hours, with cheese packs in the kits.

FDAOct 3, 2018MD• K.B. Pizza, Inc.

Cheese Pizza Kit (K.B. Pizza) – Unknown safety issue (2018)

K.B. Pizza, Inc. has initiated a recall of Son of Italy Cheese Kit, Son of Italy Pepperoni Kit, 39 oz./2 pizzas per kit, Vacuum packed, 6 kits per case. Use by date of 12-5-18 on each kit and case, because the pizza kits were left at room temperature for 24 hours, with cheese packs in the kits.

FDAOct 3, 2018MD• K.B. Pizza, Inc.

2018 KZRV SONIC Recall: EQUIPMENT:RECREATIONAL VEHICLE/TRAILER

KZRV, L.P. (KZRV) is recalling certain 2017-2019 KZRV Sonic 190VRB travel trailers. The liquid propane (LP) manifold may be located close to the axle tube, which can result in damage to the manifold, causing a leak.

NHTSASep 28, 2018Nationwide• KZRV

Abilify (Otsuka Pharmaceutical) – Mislabeling (2018)

Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW Abilify are mislabeled. Product name is misspelled, storage instructions are missing and contents of kits may be incorrectly labeled on the outer packaging of the co-packaged kit.

FDASep 17, 2018Nationwide• Otsuka Pharmaceutical Development & Commercialization, Inc.

2017 KZRV VENOM Recall: EQUIPMENT:OTHER:LABELS

KZRV, L.P. (KZRV) is recalling certain 2017-2019 KZRV Durango, Venom and Sidewinder recreational trailers. The Federal Certification label incorrectly lists the tire size as being ST235/80R16G, however, the correct tire size is ST235/85R16G.

NHTSAAug 16, 2018Nationwide• KZRV

2019 KZRV CONNECT Recall: EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:LINES AND FITTINGS

KZRV, L.P. (KZRV) is recalling certain 2018-2019 KZ RV Connect recreational trailers, model C261RL. The liquid propane lines on these vehicles are routed through the wheel well and may be damaged by road debris.

NHTSAAug 15, 2018Nationwide• KZRV