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TERBERG BENSCHOP B.V.

TERBERG BENSCHOP B.V. Recalls

All product recalls associated with TERBERG BENSCHOP B.V..

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 621–640 of 4465 recalls

Terberg Terminal Tractor (Terberg) – Axle Fastener (2023)

Terberg Benschop B.V. is recalling one 2022 YT193 terminal tractor. The eight non-self-locking flange nuts that attach the steering front axle to the front axle suspension may come loose.

NHTSANov 13, 2023Nationwide• TERBERG BENSCHOP B.V.

CORI Robotic Drill (Blue Belt) – Disconnection Errors (2023)

Possibility that the user is unable to resolve drill disconnection error messages.

FDANov 13, 2023Nationwide• Blue Belt Technologies, Inc

Tow-Behind Field Mowers (DR Power) – fire hazard (2023)

Fire/Burn Risk

This recall involves DR Power Equipment and Generac brand tow-behind field and brush mowers. The following model and serial numbers, printed on a white label that is on the rear frame of the mower near the right rear tire, are included in this recall. Name Model Number Serial Number Range DR Power Tow-Behind Field and Brush Mower TB 25044B EN All serial numbers beginning with TB2, plus 3002188267 to 30024310751 TB 25044B ENC 30030052232 to 3004525033 TB 25044B ENR 3004734233, 3004835965, 3005064288, 3005471720, 3005548665, 3007678624, 3008122643 TBM 20A ED TDVE OF1 All serial numbers beginning with TB; in addition, 300275210 TBM 20A EN TDVE OD3 All TBM 20A EN TDVE OF3 TBM20AENTDVEOF3 All 3002188263 to 3002490281 Generac Tow-Behind Field and Brush Mower TB 25044GENG 3003540054 to 3004428691

1...30 313233 34...224

Page 32 of 224Next

CPSCNov 9, 2023Nationwide• DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin (through January 2018)

LET Gel (Right Value Drug Stores) – Product Mix-up (2023)

Product Mix-up: Incorrect Product Formulation

Class IIILow

FDANov 9, 2023Nationwide• Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop

Medical System (GE) – Bolt Torque Issue (2023)

GE HealthCare has become aware of the potential that incorrect torque has been applied to certain bolts of the Definium Tempo and Definium Tempo Pro products which may result in a potential fall of elements of the Overhead Tube Suspension (OTS) assembly.

FDANov 7, 2023Nationwide• GE Hangwei Medical Systems, Co. LTD West Area Bldg. 3, No.1 Yongchang North Road 1 Yongchangbeilu; Beijing Economic and Technological Development Area Beijing China

Allura Systems (Philips) – ceiling mount collision risk (2023)

Ceiling mounted L-arm contains a rotation cover that may potentially be susceptible to falling if a collision between the L-arm and other hospital equipment (i.e., an operating light) were to occur result in injury or potential sterility issues due to the cover becoming loose

FDANov 3, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Azurion Systems (Philips) – ceiling mount collision risk (2023)

FDANov 3, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Infusomat Administration Sets (B. Braun) – tubing inconsistency (2023)

In affected products, the tubing outer diameter may vary in size or the length of tubing may be too short. Both issues may lead to false air-in-line alarms, which will stop the infusion and interrupt therapy. Interruptions or delays in medication administration may result in serious injury to patients which may be life-threatening (e.g. interruption of a vasopressor to a hemodynamically unstable patient) or may lead to death.

FDANov 1, 2023Nationwide• B. Braun Medical, Inc.

Lubricating Eye Drops (Major) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Lubricating Tears Eye Drops (Major) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Probiotic Tri-Blend (Abbott) – unapproved drug (2023)

Marketed towards preterm infants without approval as a new drug or licensed biologic, as well as unsafe food additive

Class IIModerate

FDAOct 31, 2023AL, AZ, AR +38 more• Abbott Laboratories

Alinity HCV AMP Kit (Abbott) – false positive results (2023)

Abbott has received reports of an increase in reactive negative controls and false positive results in patient samples when using the Identified Lots of Alinity m HCV AMP Kit.

FDAOct 30, 2023Nationwide• Abbott Molecular, Inc.

Bobcat Zero-Turn Lawnmowers – crash risk (2023)

Laceration Risk

This recall involves Bobcat-branded and Kubota-branded stand-on zero-turn lawnmowers. The Bobcat stand-on zero-turn lawnmowers are black and white with the Bobcat name and logo on an orange background. They also have orange wheel wells. The Kubota stand-on zero-turn lawnmowers are orange and black with the Kubota name in white and orange wheel wells. The following model and serial numbers, located on the right side of the frame just above the operator platform, are included in this recall. The recalled engines are model year 2023 FR730V, FR691V, and FR651V. The recalled engine model and serial numbers are located on the engine fan housing. The following model and serial number ranges are included in this recall. Bobcat: MODEL SERIAL NUMBER ZS4036 999400100961 thru 999400100973 999400100975 thru 999400101046 999400101049 thru 999400101053 999400101055 ZS4036 SJAU 9994001AU80157 thru 9994001AU80165 9994001AU80168 thru 9994001AU80169 ZS4048 999400201096 thru 999400201170 ZS4048 SFAU 9994002AU00141 thru 9994002AU00145 ZS4052 999400301247 thru 999400301380 999400301382 thru 999400301385 999400301387 thru 999400301397 ZS4052 SKAU 9994003AU00125 ZS4061 999400400750 thru 999400400822 999400400826 thru 999400400831 999400400833 thru 999400400834 999400400836 thru 999400400838 ZS4061 SKAU 9994004AU00111 thru 9994004AU00112 Kubota: MODEL SERIAL NUMBER SZ19NC-36-2 14490 thru 14517 14618 thru 14620 14678 thru 14679 14803 thru 14818 14835 thru 14850 14856 thru 14857 14922 thru 14927 15051 thru 15062 SZ22NC-48-2 14380 14401 thru 14412 14566 thru 14568 14666 thru 14677 14695 thru 14700 14706 thru 14711 14790 thru 14796 14858 thru 14869 14928 thru 14931 15030 thru 15044 SZ26NC-52-2 14429 thru 14446 14466 thru 14471 14474 14484 thru 14489 14577 thru 14609 14692 thru 14694 14701 thru 14705 14712 thru 14717 14780 thru 14783 14872 thru 14888 14892 14921 14944 thru 14967 14992 thru 15007 SZ26NC-61-2 14417 thru 14425 14475 thru 14483 14622 thru 14643 14718 14763 thru 14771 14893 thru 14904 14971 thru 14991 15014 thru 15026 SZ19-36-2CAD 14558 thru 14565, 14801 SZ22-48-2CAD 14569 thru 14576, 14870 thru 14871, 15045 SZ26-61-2CAD 15009 thru 15013, 15029 1698562

CPSCOct 26, 2023Nationwide• Doosan Bobcat North America, of West Fargo, North Dakota

CD11b APC (BD Biosciences) – cell staining quality (2023)

In vitro diagnostics product that impacts the quality of cell staining can cause low or dim fluorescence signal, which can lead to potential false negative results and misdiagnosis of hematological malignancy, delayed treatment, and the need for additional patient samples.

FDAOct 25, 2023Nationwide• Becton, Dickinson and Company, BD Biosciences

Phenytoin Oral Suspension (Major) – content uniformity issue (2023)

Failed Content Uniformity Specifications

Class IHigh

FDAOct 23, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Kuka Flex Forte Caplets (Botanical Be) – Undeclared Ingredient (2023)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

Class IHigh

FDAOct 20, 2023Nationwide• Botanical Be

Reumo Flex Caplets (Botanical Be) – undeclared ingredient (2023)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

Class IHigh

FDAOct 20, 2023Nationwide• Botanical Be

Artri King Reforzado Tablets (Botanical Be) – Undeclared Ingredient (2023)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

Class IHigh

FDAOct 20, 2023Nationwide• Botanical Be

ARCHITECT c4000 Processing Module (Abbott) – undeclared latex (2023)

The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).

FDAOct 19, 2023AL, AK, AZ +45 more• Abbott Laboratories

CELL-DYN Ruby (Abbott) – undeclared latex (2023)

The devices contain a dry natural rubber (latex) subcomponent, which are not labeled as containing dry natural rubber(latex).

FDAOct 19, 2023AL, AZ, AR +35 more• Abbott Laboratories