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Linet Spol. S.r.o. Zelevcice 5 Zelevcice Czech Republic

Linet Spol. S.r.o. Zelevcice 5 Zelevcice Czech Republic Recalls

All product recalls associated with Linet Spol. S.r.o. Zelevcice 5 Zelevcice Czech Republic.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 4601–4620 of 21320 recalls

Sprint 200 Stretcher (Linet) – Siderail Locking (2023)

Labeling being updated to assure user is securing the siderail to a locked position to prevent potential patient fall and injury.

Moderate

FDAJan 18, 2023AL, CA, FL +11 more• Linet Spol. S.r.o. Zelevcice 5 Zelevcice Czech Republic

IntelliVue G7m Anesthesia Module (Philips) – Gas Measurement Interruption (2023)

The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption of the gas measurement. This issue concerns the G7m's sample gas pump which could stop working, producing a technical, INOP (inoperable) alarm. The pump may fail prematurely when there is friction caused by an abrasion. This recall is for an IMPORTANT PRODUCT NOTICE dated 1/18/23.

Moderate

FDAJan 18, 2023Nationwide• Philips North America

Ohm Sanitizer Spray (Urban Electric) - Chemical Contamination (2023)

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

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Class IIModerate

FDAJan 17, 2023Nationwide• Urban Electric Power

Hand Sanitizer (Fisher) - CGMP Manufacturing Issue (2023)

CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary approval, into the market after March 31, 2022.

Class IIModerate

FDAJan 17, 2023Nationwide• Fisher Scientific Co., LLC

Hand Sanitizer (Fisher) - CGMP Manufacturing Issue (2023)

Class IIModerate

FDAJan 17, 2023Nationwide• Fisher Scientific Co., LLC

Ohm Hand Sanitizer (Urban Electric) - Chemical Contamination (2023)

CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Class IIModerate

FDAJan 17, 2023Nationwide• Urban Electric Power

Siemens Biograph Horizon (Siemens) – Gantry Locking Issue (2023)

This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

Moderate

FDAJan 16, 2023Nationwide• Siemens Medical Solutions USA, Inc.

Irvine Scientific Embryo Oil (Fujifilm) – Oil Toxicity (2023)

Due to the detection of oil toxicity in several lots of Oil for Embryo Culture products.

Moderate

FDAJan 16, 2023AZ, AR, CA +32 more• Fujifilm Irvine Scientific, Inc.

Siemens Biograph mCT (Siemens) – Gantry Locking Issue (2023)

This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

Moderate

FDAJan 16, 2023Nationwide• Siemens Medical Solutions USA, Inc.

Hologic 3Dimensions (Hologic) – C-Arm Movement Risk (2023)

C-Arm unexpected movement may cause blunt trauma should the tube arm impinge upon an individual

Moderate

FDAJan 16, 2023Nationwide• Hologic, Inc.

Siemens Biograph Vision (Siemens) – Gantry Locking Issue (2023)

This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

Moderate

FDAJan 16, 2023Nationwide• Siemens Medical Solutions USA, Inc.

Allopurinol Tablets (Preferred) - Foreign Substance (2023)

Presence of Foreign Substance: manufacturer recalled this re-packaged product due to reports of a small piece of green plastic embedded in the crack towards the edge of the tablet.

Class IIModerate

FDAJan 16, 2023IN• Preferred Pharmaceuticals, Inc.

Nasal Septal Button (Summit Medical) – Unsealed Pouches (2023)

Sterile product pouches were not sealed.

Moderate

FDAJan 13, 2023CO, FL, GA +3 more• Summit Medical, LLC

Diltiazem Hydrochloride Capsules (Sun) - Impurity Failure (2023)

Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during stability testing and failed dissolution testing at FDA laboratory.

Class IIModerate

FDAJan 13, 2023Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Honda Talon 1000 ROVs (Honda) - crash hazard (2023)

This recall expansion involves an additional 2,000 2021 model year Honda Talon 1000 side-by-sides with model numbers Talon 1000 S2 and Talon 1000 S4. The vehicles were sold in various colors including red, blue, green, gray and yellow. "HONDA" is printed on the front, sides and the rear of each vehicle. "Talon" is printed on a label located on both sides of the vehicle. The Vehicle Identification Number (VIN) number is stamped on the frame on the left side under the left front fender. The VIN range for affected Talon 1000s is as shown below. Original Recall: MY Model VIN Start VIN End 2019 Talon 1000 S2 1HFVE05**K4000003 1HFVE05**K4003902 2020 Talon 1000 S2 1HFVE05**L4100001 1HFVE05**L4102280 2021 Talon 1000 S2 1HFVE05**M4200001 1HFVE05**M4202760 2020 Talon 1000 S4 1HFVE06**L4000002 1HFVE06**L4003420 2021 Talon 1000 S4 1HFVE06**M4100001 1HFVE06**M4102218 Expanded Recall: : MY Model VIN Start VIN End 2019 Talon 1000 S2 1HFVE05**M4200084 1HFVE05**M4203061 2020 Talon 1000 S4 1HFVE06**M4100121 1HFVE06**M4102580

Moderate

CPSCJan 12, 2023Nationwide• American Honda Motor Co. Inc., of Torrance, California

86-Inch Smart TVs (LG Electronics) – Tip-Over Hazard (2023)

This recall involves four LG Electronics 86-inch smart TV models with model numbers 86UQ8000AUB, 86UQ7070ZUD, 86UQ7590PUD, and 86NANO75UQA. The TVs (not including the stands) are 86 inches diagonally, 43.5 inches high, 76 inches wide, and 2.4 inches deep. They weigh approximately 100 pounds. The serial number of the recalled product begins with 202RM, 203RM, 204RM, 205RM, 206RM, 207RM, or 208RM and is located at the bottom right of the back of the TV, along with the model number. Consumers can also check the serial number by pressing the mute button, three times rapidly, on the original LG remote control provided with their TV.

Very High

CPSCJan 12, 2023Nationwide• LG Electronics Reynosa, S.A. de C.V., of Reynosa, Mexico

Metoprolol Succinate Tablets (Amerisource) - Dissolution Failure (2023)

Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories.

Class IIModerate

FDAJan 11, 2023Nationwide• Amerisource Health Services LLC